FAM193A
family with sequence similarity 193 member A
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs150209965 | 4:2,554,715 | C/T | intron variant | — |
| rs542777826 | 4:2,566,944 | T/C | — | — |
| rs142467211 | 4:2,567,695 | A/T | intron variant | — |
| rs145959580 | 4:2,632,760 | C/T | — | uncertain significance |
| rs770236370 | 4:2,632,846 | G/A | — | uncertain significance |
| rs199976101 | 4:2,641,568 | C/T | — | uncertain significance |
| rs781076887 | 4:2,648,440 | A/G | — | uncertain significance |
| rs142464183 | 4:2,648,449 | A/G | — | uncertain significance |
| rs2529666098 | 4:2,648,471 | G/A | — | uncertain significance |
| rs780608278 | 4:2,659,552 | G/A | — | uncertain significance |
| rs751420434 | 4:2,659,601 | A/T | — | uncertain significance |
| rs2529725334 | 4:2,661,300 | G/A | — | uncertain significance |
| rs149282262 | 4:2,661,355 | G/A | — | uncertain significance |
| rs550227977 | 4:2,661,769 | C/T | — | uncertain significance |
| rs1192906300 | 4:2,664,629 | A/G | — | uncertain significance |
| rs1712640705 | 4:2,664,647 | G/T | — | uncertain significance |
| rs1181788489 | 4:2,664,881 | G/A | — | uncertain significance |
| rs34782960 | 4:2,664,974 | A/G | — | benign |
| rs1290933 | 4:2,668,217 | C/A | intron variant | — |
| rs1440151336 | 4:2,673,857 | G/A | — | uncertain significance |
| rs974973924 | 4:2,673,909 | C/T | — | uncertain significance |
| rs1450058447 | 4:2,673,915 | C/T | — | uncertain significance |
| rs777954987 | 4:2,673,929 | G/A | — | uncertain significance |
| rs2529787409 | 4:2,673,992 | C/G | — | uncertain significance |
| rs372896676 | 4:2,674,047 | G/A | — | uncertain significance |
| rs372731013 | 4:2,674,095 | G/C | — | uncertain significance |
| rs17164088 | 4:2,675,893 | A/C | — | — |
| rs2529896095 | 4:2,692,439 | G/A | — | uncertain significance |
| rs757652109 | 4:2,692,580 | G/A | — | uncertain significance |
| rs79752154 | 4:2,692,704 | C/T | — | benign |
| rs1396416544 | 4:2,695,363 | G/T | — | uncertain significance |
| rs745620965 | 4:2,695,393 | G/T | — | uncertain significance |
| rs753909067 | 4:2,695,421 | C/T | — | uncertain significance |
| rs1431006948 | 4:2,695,490 | C/T | — | uncertain significance |
| rs2529917140 | 4:2,695,523 | A/T | — | uncertain significance |
| rs373317366 | 4:2,695,529 | G/T | — | uncertain significance |
| rs748732999 | 4:2,695,589 | C/A | — | uncertain significance |
| rs767342735 | 4:2,696,695 | C/T | — | uncertain significance |
| rs149980051 | 4:2,696,701 | G/A | — | uncertain significance |
| rs781488456 | 4:2,696,723 | A/C | — | uncertain significance |
| rs182204199 | 4:2,698,213 | G/A | — | uncertain significance |
| rs990427318 | 4:2,698,228 | G/T | — | uncertain significance |
| rs2529954187 | 4:2,701,461 | C/T | — | uncertain significance |
| rs763043929 | 4:2,701,519 | G/A | — | uncertain significance |
| rs1717491732 | 4:2,701,539 | C/T | — | uncertain significance |
| rs771325069 | 4:2,701,564 | G/A | — | uncertain significance |
| rs1717504898 | 4:2,701,626 | A/C | — | uncertain significance |
| rs146890120 | 4:2,701,681 | A/G | — | uncertain significance |
| rs777239950 | 4:2,701,741 | T/G | — | uncertain significance |
| rs1717523422 | 4:2,701,745 | C/G | — | uncertain significance |
| rs201303704 | 4:2,701,750 | C/T | — | uncertain significance |
| rs2529956692 | 4:2,701,762 | C/G | — | uncertain significance |
| rs148532447 | 4:2,701,797 | G/A | — | uncertain significance |
| rs537047866 | 4:2,701,951 | C/A | — | uncertain significance |
| rs1298861410 | 4:2,701,968 | C/T | — | uncertain significance |
| rs375143004 | 4:2,702,002 | G/A | — | uncertain significance |
| rs367937347 | 4:2,702,011 | C/T | — | uncertain significance |
| rs776408003 | 4:2,702,136 | C/T | — | uncertain significance |
| rs1169839258 | 4:2,717,786 | G/C | — | uncertain significance |
| rs534197687 | 4:2,721,742 | G/A | — | likely benign |
| rs4690028 | 4:2,722,793 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.