KIAA1671
KIAA1671
Summary
Located in cilium; intercellular bridge; and microtubule cytoskeleton. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants123 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs147994709 | 22:25,395,685 | A/C | intron variant | — |
| rs1284441781 | 22:25,424,012 | G/A | — | uncertain significance |
| rs1926047034 | 22:25,424,015 | C/G | — | uncertain significance |
| rs1926047296 | 22:25,424,016 | C/A | — | uncertain significance |
| rs968632121 | 22:25,424,070 | A/G | — | uncertain significance |
| rs939387953 | 22:25,424,211 | C/T | — | uncertain significance |
| rs1250598128 | 22:25,424,352 | C/G | — | uncertain significance |
| rs972924232 | 22:25,424,402 | C/T | — | uncertain significance |
| rs2517607916 | 22:25,424,420 | A/C | — | uncertain significance |
| rs367983522 | 22:25,424,429 | G/A | — | likely benign |
| rs1276153240 | 22:25,424,442 | C/A | — | uncertain significance |
| rs866531061 | 22:25,424,465 | G/T | — | uncertain significance |
| rs1384786280 | 22:25,424,538 | G/A | — | uncertain significance |
| rs1191008027 | 22:25,424,549 | C/T | — | uncertain significance |
| rs973340896 | 22:25,424,591 | C/G | — | uncertain significance |
| rs370932896 | 22:25,424,601 | C/G | — | uncertain significance |
| rs1489604686 | 22:25,424,646 | C/T | — | uncertain significance |
| rs1191243812 | 22:25,424,741 | G/C | — | uncertain significance |
| rs534336780 | 22:25,424,830 | G/A | — | likely benign |
| rs957022850 | 22:25,424,949 | A/G | — | uncertain significance |
| rs554100016 | 22:25,424,973 | C/T | — | uncertain significance |
| rs1488913794 | 22:25,425,087 | C/T | — | uncertain significance |
| rs1277412840 | 22:25,425,117 | G/C | — | uncertain significance |
| rs1341905753 | 22:25,425,130 | A/C | — | uncertain significance |
| rs1926129082 | 22:25,425,164 | G/T | — | uncertain significance |
| rs1001531741 | 22:25,425,300 | G/T | — | uncertain significance |
| rs954795425 | 22:25,425,339 | C/T | — | uncertain significance |
| rs1257724112 | 22:25,425,369 | C/T | — | likely benign |
| rs200771652 | 22:25,425,430 | C/T | — | likely benign |
| rs868505122 | 22:25,425,463 | G/T | — | uncertain significance |
| rs1195150085 | 22:25,425,468 | C/T | — | uncertain significance |
| rs1926357332 | 22:25,428,646 | A/G | — | uncertain significance |
| rs778689439 | 22:25,434,764 | C/T | — | uncertain significance |
| rs929984157 | 22:25,434,793 | C/T | — | uncertain significance |
| rs1198577896 | 22:25,434,801 | G/T | — | uncertain significance |
| rs1033366857 | 22:25,434,911 | G/A | — | uncertain significance |
| rs1226547347 | 22:25,434,948 | C/G | — | uncertain significance |
| rs202182154 | 22:25,435,012 | G/A | — | uncertain significance |
| rs1249830294 | 22:25,435,025 | C/T | — | uncertain significance |
| rs905260840 | 22:25,435,039 | C/T | — | uncertain significance |
| rs955078332 | 22:25,435,139 | C/T | — | likely benign |
| rs1366425643 | 22:25,435,184 | C/T | — | uncertain significance |
| rs974653850 | 22:25,435,189 | C/T | — | uncertain significance |
| rs1926783115 | 22:25,435,218 | G/C | — | uncertain significance |
| rs530114371 | 22:25,435,226 | A/G | — | uncertain significance |
| rs973261086 | 22:25,435,274 | C/T | — | uncertain significance |
| rs1812448387 | 22:25,435,289 | C/A | — | uncertain significance |
| rs75885201 | 22:25,435,336 | G/A | — | uncertain significance |
| rs1926790735 | 22:25,435,337 | C/A | — | uncertain significance |
| rs868750654 | 22:25,435,375 | C/T | — | uncertain significance |
| rs982929799 | 22:25,435,381 | C/G | — | uncertain significance |
| rs926572934 | 22:25,435,475 | T/A | — | uncertain significance |
| rs1926810511 | 22:25,435,732 | C/T | — | uncertain significance |
| rs970971940 | 22:25,435,750 | G/A | — | uncertain significance |
| rs367786792 | 22:25,435,868 | C/T | — | uncertain significance |
| rs866957194 | 22:25,435,871 | C/T | — | uncertain significance |
| rs886871438 | 22:25,435,909 | G/C | — | uncertain significance |
| rs1926824695 | 22:25,435,957 | C/G | — | uncertain significance |
| rs1164492580 | 22:25,435,961 | A/G | — | uncertain significance |
| rs1033961845 | 22:25,436,003 | C/T | — | uncertain significance |
| rs1021342087 | 22:25,436,039 | G/A | — | uncertain significance |
| rs1419930566 | 22:25,436,099 | A/G | — | uncertain significance |
| rs2517626323 | 22:25,436,101 | G/T | — | uncertain significance |
| rs2145806016 | 22:25,436,106 | C/G | — | uncertain significance |
| rs1461255869 | 22:25,436,399 | A/G | — | uncertain significance |
| rs927703889 | 22:25,436,419 | C/T | — | uncertain significance |
| rs1043061088 | 22:25,436,518 | C/T | — | uncertain significance |
| rs2517627277 | 22:25,436,556 | G/A | — | likely benign |
| rs1015530649 | 22:25,436,588 | C/T | — | uncertain significance |
| rs2517627380 | 22:25,436,594 | T/C | — | uncertain significance |
| rs1389297933 | 22:25,436,602 | C/T | — | uncertain significance |
| rs199826422 | 22:25,436,689 | G/A | — | uncertain significance |
| rs1236512295 | 22:25,436,729 | T/C | — | uncertain significance |
| rs78336891 | 22:25,436,765 | G/A | — | uncertain significance |
| rs2517627695 | 22:25,436,776 | G/A | — | uncertain significance |
| rs1483946333 | 22:25,436,797 | C/T | — | uncertain significance |
| rs1473994213 | 22:25,436,805 | G/T | — | uncertain significance |
| rs200060948 | 22:25,436,821 | G/A | — | uncertain significance |
| rs1381681348 | 22:25,436,831 | A/G | — | uncertain significance |
| rs577924119 | 22:25,436,852 | A/G | — | uncertain significance |
| rs200775683 | 22:25,436,977 | C/T | — | uncertain significance |
| rs2517628141 | 22:25,437,001 | T/C | — | uncertain significance |
| rs1409317086 | 22:25,437,017 | G/A | — | likely benign |
| rs867947486 | 22:25,437,026 | G/T | — | uncertain significance |
| rs1367825621 | 22:25,437,113 | C/T | — | uncertain significance |
| rs761045180 | 22:25,437,173 | G/A | — | uncertain significance |
| rs1311183718 | 22:25,437,208 | C/G | — | uncertain significance |
| rs1176924605 | 22:25,437,241 | C/T | — | uncertain significance |
| rs1358676712 | 22:25,437,302 | C/T | — | uncertain significance |
| rs2517628916 | 22:25,437,388 | A/T | — | uncertain significance |
| rs1926922465 | 22:25,437,485 | G/T | — | uncertain significance |
| rs773899261 | 22:25,445,249 | C/T | — | uncertain significance |
| rs1239801707 | 22:25,445,282 | C/T | — | uncertain significance |
| rs1211695037 | 22:25,445,302 | T/C | — | uncertain significance |
| rs1602098235 | 22:25,445,317 | A/C | — | uncertain significance |
| rs184105678 | 22:25,466,418 | G/A | regulatory region variant | — |
| rs5760860 | 22:25,505,936 | A/C | intron variant | — |
| rs542161264 | 22:25,514,537 | C/T | — | — |
| rs1413756757 | 22:25,566,842 | C/T | — | uncertain significance |
| rs552025293 | 22:25,566,847 | G/A | — | uncertain significance |
Showing 100 of 123 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.