FAM184B
family with sequence similarity 184 member B
Known Variants83 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs916540890 | 4:17,634,216 | T/G | — | uncertain significance |
| rs530767348 | 4:17,635,363 | C/T | — | uncertain significance |
| rs202198134 | 4:17,635,400 | T/C | — | uncertain significance |
| rs1221058083 | 4:17,635,411 | T/C | — | uncertain significance |
| rs374104756 | 4:17,635,416 | C/G | — | uncertain significance |
| rs368263511 | 4:17,635,430 | C/T | — | uncertain significance |
| rs1448409766 | 4:17,635,435 | C/A | — | uncertain significance |
| rs1357084381 | 4:17,635,468 | G/A | — | uncertain significance |
| rs183471400 | 4:17,635,481 | C/T | — | uncertain significance |
| rs368942670 | 4:17,635,483 | C/T | — | uncertain significance |
| rs1464387513 | 4:17,635,487 | T/C | — | uncertain significance |
| rs1037962319 | 4:17,635,501 | A/G | — | uncertain significance |
| rs1392152441 | 4:17,636,682 | G/A | — | uncertain significance |
| rs143581443 | 4:17,636,687 | C/T | — | uncertain significance |
| rs1208696381 | 4:17,638,152 | G/A | — | uncertain significance |
| rs926027663 | 4:17,638,176 | C/T | — | uncertain significance |
| rs530812460 | 4:17,638,206 | A/G | — | uncertain significance |
| rs774679756 | 4:17,638,250 | C/G | — | uncertain significance |
| rs1332383479 | 4:17,640,936 | A/G | — | uncertain significance |
| rs758159377 | 4:17,640,990 | C/T | — | uncertain significance |
| rs1323776088 | 4:17,643,728 | C/G | — | uncertain significance |
| rs2108930907 | 4:17,643,752 | C/T | — | uncertain significance |
| rs887243309 | 4:17,643,817 | G/A | — | uncertain significance |
| rs772721882 | 4:17,643,847 | C/T | — | uncertain significance |
| rs1310267058 | 4:17,643,850 | T/C | — | uncertain significance |
| rs1374487935 | 4:17,643,851 | C/T | — | uncertain significance |
| rs1715508645 | 4:17,649,367 | G/A | — | uncertain significance |
| rs116972792 | 4:17,650,417 | G/A | intron variant | — |
| rs186084989 | 4:17,654,542 | C/T | — | uncertain significance |
| rs769065857 | 4:17,654,573 | G/A | — | uncertain significance |
| rs1475825711 | 4:17,654,599 | T/C | — | uncertain significance |
| rs1294216625 | 4:17,659,978 | G/T | — | uncertain significance |
| rs2474523986 | 4:17,660,026 | A/G | — | uncertain significance |
| rs774253383 | 4:17,660,032 | C/T | — | uncertain significance |
| rs574728573 | 4:17,660,047 | T/A | — | uncertain significance |
| rs563589893 | 4:17,660,054 | G/C | — | uncertain significance |
| rs2474525660 | 4:17,661,612 | C/A | — | uncertain significance |
| rs908356099 | 4:17,661,637 | T/C | — | likely benign |
| rs369083060 | 4:17,661,664 | C/G | — | uncertain significance |
| rs1476835 | 4:17,665,456 | C/T | intron variant | — |
| rs1018345075 | 4:17,666,243 | C/G | — | uncertain significance |
| rs1231028117 | 4:17,666,245 | C/A | — | uncertain significance |
| rs550571596 | 4:17,675,659 | T/A | — | — |
| rs1008375 | 4:17,682,834 | T/A | — | — |
| rs1024982309 | 4:17,690,061 | T/A | — | uncertain significance |
| rs767851786 | 4:17,690,075 | C/T | — | uncertain significance |
| rs777630378 | 4:17,690,114 | C/T | — | uncertain significance |
| rs796811510 | 4:17,690,115 | G/A | — | likely benign |
| rs2474556311 | 4:17,690,132 | A/G | — | uncertain significance |
| rs1437838670 | 4:17,694,962 | G/A | — | uncertain significance |
| rs141014192 | 4:17,696,804 | C/G | intron variant | — |
| rs756474638 | 4:17,706,661 | G/A | — | uncertain significance |
| rs369981718 | 4:17,706,679 | C/T | — | uncertain significance |
| rs916410883 | 4:17,706,718 | G/C | — | uncertain significance |
| rs13139898 | 4:17,706,928 | T/G | intron variant | — |
| rs1033460337 | 4:17,707,378 | C/T | — | uncertain significance |
| rs536804026 | 4:17,707,431 | G/T | — | uncertain significance |
| rs192178401 | 4:17,707,472 | C/G | — | likely benign |
| rs61741465 | 4:17,707,473 | G/A | — | uncertain significance |
| rs1189072122 | 4:17,707,498 | C/A | — | uncertain significance |
| rs1368503433 | 4:17,707,507 | C/T | — | uncertain significance |
| rs1181143684 | 4:17,709,275 | T/C | — | uncertain significance |
| rs370275592 | 4:17,709,289 | C/T | — | likely benign |
| rs975346362 | 4:17,709,290 | G/A | — | uncertain significance |
| rs2474575962 | 4:17,709,343 | T/A | — | uncertain significance |
| rs1291576220 | 4:17,710,571 | C/A | — | uncertain significance |
| rs1371832197 | 4:17,710,645 | C/G | — | uncertain significance |
| rs988361612 | 4:17,710,682 | C/T | — | uncertain significance |
| rs1214275859 | 4:17,710,702 | A/G | — | uncertain significance |
| rs1222367318 | 4:17,710,762 | C/T | — | uncertain significance |
| rs1281355068 | 4:17,710,766 | C/T | — | uncertain significance |
| rs1320113146 | 4:17,710,885 | C/T | — | uncertain significance |
| rs79121259 | 4:17,710,905 | G/C | missense variant | — |
| rs1266723739 | 4:17,710,969 | A/G | — | uncertain significance |
| rs1717196291 | 4:17,711,008 | A/G | — | uncertain significance |
| rs1035757642 | 4:17,711,011 | T/A | — | uncertain significance |
| rs564470488 | 4:17,711,031 | C/T | — | likely benign |
| rs1019585445 | 4:17,711,098 | A/G | — | uncertain significance |
| rs1436480313 | 4:17,711,159 | T/C | — | uncertain significance |
| rs907182839 | 4:17,711,194 | T/C | — | uncertain significance |
| rs1002901986 | 4:17,711,199 | G/T | — | uncertain significance |
| rs61746445 | 4:17,711,210 | G/A | — | likely benign |
| rs2109045 | 4:17,759,311 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.