FAM171B
family with sequence similarity 171 member B
Summary
Predicted to be located in membrane. Predicted to be active in synapse. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs140891434 | 2:187,558,952 | G/T | — | uncertain significance |
| rs73979342 | 2:187,559,047 | G/A | — | benign |
| rs151201990 | 2:187,559,081 | G/A | — | uncertain significance |
| rs750932658 | 2:187,559,099 | A/G | — | uncertain significance |
| rs55666589 | 2:187,569,492 | T/A | — | — |
| rs4666712 | 2:187,572,569 | A/T | — | — |
| rs552360583 | 2:187,577,173 | A/G | — | — |
| rs11683459 | 2:187,601,639 | G/A | intron variant | — |
| rs1044058581 | 2:187,604,955 | T/C | — | uncertain significance |
| rs73979354 | 2:187,605,000 | G/A | — | benign |
| rs112566975 | 2:187,605,046 | G/A | — | benign |
| rs200992002 | 2:187,605,123 | C/T | — | uncertain significance |
| rs2468552422 | 2:187,611,858 | T/C | — | uncertain significance |
| rs79964543 | 2:187,615,884 | C/T | — | benign |
| rs2468559147 | 2:187,615,930 | T/C | — | uncertain significance |
| rs1333540703 | 2:187,615,932 | A/C | — | uncertain significance |
| rs371787365 | 2:187,615,947 | A/G | — | uncertain significance |
| rs374154235 | 2:187,615,963 | C/T | — | uncertain significance |
| rs748120054 | 2:187,616,007 | G/T | — | uncertain significance |
| rs148611836 | 2:187,616,022 | A/G | — | uncertain significance |
| rs201265058 | 2:187,618,701 | A/G | — | uncertain significance |
| rs200396345 | 2:187,618,768 | G/A | — | uncertain significance |
| rs2468574765 | 2:187,626,417 | A/G | — | uncertain significance |
| rs2468574852 | 2:187,626,460 | A/G | — | uncertain significance |
| rs781557815 | 2:187,626,489 | C/A | — | uncertain significance |
| rs771014656 | 2:187,626,532 | A/G | — | likely benign |
| rs760544489 | 2:187,626,549 | C/A | — | uncertain significance |
| rs75100182 | 2:187,626,632 | G/A | — | benign |
| rs778222422 | 2:187,626,726 | C/A | — | uncertain significance |
| rs772260065 | 2:187,626,774 | G/A | — | uncertain significance |
| rs145287585 | 2:187,626,805 | G/A | — | uncertain significance |
| rs1690629033 | 2:187,626,937 | A/T | — | uncertain significance |
| rs1199502753 | 2:187,627,405 | C/T | — | uncertain significance |
| rs761365421 | 2:187,627,456 | C/G | — | uncertain significance |
| rs181761114 | 2:187,627,477 | C/A | — | uncertain significance |
| rs145896997 | 2:187,627,528 | G/A | — | uncertain significance |
| rs75409893 | 2:187,627,541 | C/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.