DISP2
dispatched RND transporter family member 2
Summary
This gene is one of two human homologs of a segment-polarity gene known as dispatched identified in Drosophila. The product of this gene may be required for normal Hedgehog (Hh) signaling during embryonic pattern formation. [provided by RefSeq, Jan 2017]
Known Variants103 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs905432053 | 15:40,650,529 | G/A | — | uncertain significance |
| rs941450336 | 15:40,650,542 | G/C | — | uncertain significance |
| rs12594374 | 15:40,650,547 | A/G | — | uncertain significance |
| rs1032606830 | 15:40,650,565 | G/A | — | uncertain significance |
| rs1017999621 | 15:40,650,634 | C/G | — | uncertain significance |
| rs1188431484 | 15:40,650,635 | C/G | — | uncertain significance |
| rs146107339 | 15:40,655,980 | C/T | — | uncertain significance |
| rs1349590834 | 15:40,655,990 | A/G | — | uncertain significance |
| rs139247330 | 15:40,655,995 | C/T | — | uncertain significance |
| rs750724751 | 15:40,656,005 | A/C | — | uncertain significance |
| rs1192958553 | 15:40,656,007 | G/C | — | uncertain significance |
| rs201394554 | 15:40,656,014 | A/C | — | likely benign |
| rs775541754 | 15:40,656,622 | C/A | — | uncertain significance |
| rs72733418 | 15:40,656,724 | T/C | — | benign |
| rs2542554575 | 15:40,656,734 | A/G | — | uncertain significance |
| rs763167909 | 15:40,657,051 | C/T | — | uncertain significance |
| rs75422658 | 15:40,657,062 | C/T | — | likely benign |
| rs764624137 | 15:40,657,081 | G/A | — | likely benign |
| rs752216408 | 15:40,657,353 | G/T | — | uncertain significance |
| rs1566914976 | 15:40,657,371 | G/C | — | uncertain significance |
| rs1404323622 | 15:40,657,379 | C/T | — | uncertain significance |
| rs1465196179 | 15:40,657,383 | G/A | — | uncertain significance |
| rs2542555767 | 15:40,657,389 | G/C | — | uncertain significance |
| rs775657161 | 15:40,657,403 | G/A | — | uncertain significance |
| rs148317482 | 15:40,657,409 | C/G | — | uncertain significance |
| rs777051988 | 15:40,657,410 | G/A | — | uncertain significance |
| rs141422641 | 15:40,657,415 | C/T | — | uncertain significance |
| rs370629806 | 15:40,657,416 | G/A | — | uncertain significance |
| rs2542556617 | 15:40,657,850 | T/C | — | uncertain significance |
| rs750207488 | 15:40,657,884 | C/A | — | uncertain significance |
| rs1889487554 | 15:40,657,912 | A/G | — | uncertain significance |
| rs535155561 | 15:40,659,301 | G/A | — | uncertain significance |
| rs369585136 | 15:40,659,362 | G/A | — | uncertain significance |
| rs774396803 | 15:40,659,410 | C/T | — | uncertain significance |
| rs1411509545 | 15:40,659,427 | G/A | — | uncertain significance |
| rs2542558489 | 15:40,659,512 | C/T | — | uncertain significance |
| rs75971826 | 15:40,659,647 | G/A | — | uncertain significance |
| rs371735197 | 15:40,659,676 | C/T | — | uncertain significance |
| rs374719365 | 15:40,659,677 | G/A | — | uncertain significance |
| rs1429952514 | 15:40,659,679 | C/A | — | uncertain significance |
| rs377372901 | 15:40,659,683 | C/T | — | conflicting classifications of pathogenicity |
| rs2542558864 | 15:40,659,729 | G/T | — | uncertain significance |
| rs143680406 | 15:40,659,743 | A/G | — | uncertain significance |
| rs1248682824 | 15:40,659,806 | C/T | — | uncertain significance |
| rs1363878785 | 15:40,659,944 | A/G | — | uncertain significance |
| rs1889529525 | 15:40,660,003 | G/C | — | uncertain significance |
| rs1399885931 | 15:40,660,034 | C/T | — | uncertain significance |
| rs139541441 | 15:40,660,039 | G/C | — | uncertain significance |
| rs761221574 | 15:40,660,040 | G/C | — | uncertain significance |
| rs779575811 | 15:40,660,139 | T/G | — | uncertain significance |
| rs1011905367 | 15:40,660,168 | G/A | — | uncertain significance |
| rs773229796 | 15:40,660,184 | C/T | — | uncertain significance |
| rs1351947062 | 15:40,660,243 | C/A | — | uncertain significance |
| rs1337228419 | 15:40,660,282 | C/T | — | uncertain significance |
| rs1185993309 | 15:40,660,300 | A/G | — | uncertain significance |
| rs2542560606 | 15:40,660,303 | G/C | — | uncertain significance |
| rs1173186288 | 15:40,660,402 | T/C | — | uncertain significance |
| rs756663851 | 15:40,660,505 | C/T | — | uncertain significance |
| rs199718039 | 15:40,660,522 | G/A | — | uncertain significance |
| rs372840873 | 15:40,660,528 | G/A | — | uncertain significance |
| rs766963535 | 15:40,660,535 | G/C | — | uncertain significance |
| rs779924295 | 15:40,660,564 | G/T | — | uncertain significance |
| rs2542561513 | 15:40,660,568 | A/C | — | uncertain significance |
| rs1417316825 | 15:40,660,769 | C/T | — | uncertain significance |
| rs779179441 | 15:40,660,771 | C/G | — | uncertain significance |
| rs140567926 | 15:40,660,807 | T/A | — | uncertain significance |
| rs201602512 | 15:40,660,824 | C/G | — | uncertain significance |
| rs764037590 | 15:40,660,840 | C/T | — | uncertain significance |
| rs1889564212 | 15:40,660,853 | G/C | — | uncertain significance |
| rs779995639 | 15:40,660,891 | G/A | — | uncertain significance |
| rs916200194 | 15:40,660,993 | T/G | — | uncertain significance |
| rs2542562526 | 15:40,661,009 | G/A | — | likely benign |
| rs1365905905 | 15:40,661,066 | A/T | — | uncertain significance |
| rs751321669 | 15:40,661,263 | T/C | — | uncertain significance |
| rs2542563105 | 15:40,661,265 | G/C | — | uncertain significance |
| rs2542563365 | 15:40,661,366 | A/G | — | uncertain significance |
| rs1373297982 | 15:40,661,435 | A/G | — | uncertain significance |
| rs371961792 | 15:40,661,470 | G/A | — | uncertain significance |
| rs139523863 | 15:40,661,567 | A/G | — | uncertain significance |
| rs1889589658 | 15:40,661,595 | G/A | — | uncertain significance |
| rs376137592 | 15:40,661,723 | G/C | — | uncertain significance |
| rs753978279 | 15:40,661,771 | G/A | — | uncertain significance |
| rs780434126 | 15:40,661,794 | G/A | — | uncertain significance |
| rs139662420 | 15:40,661,821 | C/T | — | uncertain significance |
| rs748888513 | 15:40,661,822 | G/A | — | uncertain significance |
| rs770536436 | 15:40,661,824 | C/T | — | uncertain significance |
| rs200105296 | 15:40,661,828 | G/A | — | uncertain significance |
| rs199820901 | 15:40,661,918 | C/T | — | uncertain significance |
| rs776545634 | 15:40,661,924 | G/A | — | uncertain significance |
| rs1353115233 | 15:40,661,929 | C/T | — | uncertain significance |
| rs146580728 | 15:40,661,942 | C/G | — | uncertain significance |
| rs763148128 | 15:40,662,041 | G/T | — | uncertain significance |
| rs145027994 | 15:40,662,077 | A/G | — | uncertain significance |
| rs1334099328 | 15:40,662,148 | C/T | — | uncertain significance |
| rs764410796 | 15:40,662,164 | C/T | — | uncertain significance |
| rs199950273 | 15:40,662,172 | A/G | — | uncertain significance |
| rs374170793 | 15:40,662,185 | G/A | — | uncertain significance |
| rs377610851 | 15:40,662,193 | G/A | — | uncertain significance |
| rs143167738 | 15:40,662,236 | G/A | — | uncertain significance |
| rs370968719 | 15:40,662,242 | C/G | — | uncertain significance |
Showing 100 of 103 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.