FAM13A
family with sequence similarity 13 member A
Summary
Predicted to enable GTPase activator activity. Predicted to be involved in regulation of small GTPase mediated signal transduction. Predicted to be located in cytosol. Implicated in chronic obstructive pulmonary disease. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants124 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs942316220 | 4:89,369,333 | T/C | — | association |
| rs1059122 | 4:89,647,424 | T/G | — | — |
| rs2602120 | 4:89,647,980 | C/A | — | — |
| rs3017895 | 4:89,649,491 | A/G | coding sequence variant | — |
| rs9224 | 4:89,649,659 | A/G | coding sequence variant | — |
| rs140140106 | 4:89,653,205 | G/A | — | uncertain significance |
| rs79098511 | 4:89,653,242 | G/A | — | benign |
| rs746578378 | 4:89,653,280 | A/T | — | uncertain significance |
| rs2904162 | 4:89,656,625 | A/C | intron variant | — |
| rs757593108 | 4:89,660,252 | T/G | — | uncertain significance |
| rs2602116 | 4:89,666,776 | G/A | intron variant | — |
| rs377446507 | 4:89,668,084 | G/A | — | conflicting classifications of pathogenicity |
| rs750725214 | 4:89,668,133 | C/T | — | uncertain significance |
| rs2476954583 | 4:89,668,136 | T/C | — | uncertain significance |
| rs74387785 | 4:89,668,798 | C/T | — | likely benign |
| rs1223331892 | 4:89,668,804 | C/T | — | uncertain significance |
| rs557334929 | 4:89,668,813 | C/T | — | uncertain significance |
| rs200625659 | 4:89,668,816 | T/A | — | uncertain significance |
| rs7657817 | 4:89,668,859 | C/A | missense variant | — |
| rs1221890272 | 4:89,668,913 | C/G | — | uncertain significance |
| rs28673752 | 4:89,669,874 | C/T | intron variant | — |
| rs3756050 | 4:89,670,155 | C/T | synonymous variant | — |
| rs2477028884 | 4:89,670,160 | T/G | — | uncertain significance |
| rs779417543 | 4:89,670,962 | C/T | — | uncertain significance |
| rs748582424 | 4:89,670,963 | G/A | — | uncertain significance |
| rs185686238 | 4:89,670,995 | G/C | — | uncertain significance |
| rs1321426872 | 4:89,671,034 | T/C | — | uncertain significance |
| rs2477089822 | 4:89,671,602 | G/A | — | uncertain significance |
| rs771785728 | 4:89,671,651 | C/T | — | uncertain significance |
| rs373845549 | 4:89,671,678 | C/T | — | uncertain significance |
| rs368624667 | 4:89,671,701 | C/T | — | uncertain significance |
| rs2477096936 | 4:89,671,740 | T/A | — | uncertain significance |
| rs202089420 | 4:89,671,745 | G/C | — | uncertain significance |
| rs766635116 | 4:89,671,758 | C/G | — | uncertain significance |
| rs551404204 | 4:89,671,761 | T/G | — | likely benign |
| rs370350543 | 4:89,671,782 | A/G | — | uncertain significance |
| rs1452904 | 4:89,679,648 | G/T | — | — |
| rs148685072 | 4:89,679,997 | C/A | — | uncertain significance |
| rs370681080 | 4:89,702,347 | G/A | — | uncertain significance |
| rs116703634 | 4:89,702,371 | C/T | — | uncertain significance |
| rs149660087 | 4:89,702,495 | T/C | — | uncertain significance |
| rs9992067 | 4:89,702,992 | G/C | — | — |
| rs987469 | 4:89,706,643 | C/G | intron variant | — |
| rs2869947 | 4:89,707,875 | G/T | — | — |
| rs772792148 | 4:89,708,909 | T/A | — | uncertain significance |
| rs1474304861 | 4:89,708,933 | C/A | — | uncertain significance |
| rs370204602 | 4:89,708,949 | C/T | — | uncertain significance |
| rs527746062 | 4:89,708,950 | G/A | — | uncertain significance |
| rs746457484 | 4:89,709,048 | T/C | — | uncertain significance |
| rs3822076 | 4:89,709,908 | T/A | intron variant | — |
| rs10428504 | 4:89,716,933 | G/T | intron variant | — |
| rs2869948 | 4:89,721,332 | T/C | intron variant | — |
| rs6824451 | 4:89,723,065 | G/T | — | — |
| rs10012528 | 4:89,724,963 | C/T | — | — |
| rs10012624 | 4:89,725,056 | C/T | — | — |
| rs10020704 | 4:89,725,466 | A/C | intron variant | — |
| rs1870339 | 4:89,727,656 | G/A | — | — |
| rs2167750 | 4:89,730,074 | C/T | intron variant | — |
| rs7697644 | 4:89,732,876 | C/A | — | — |
| rs6532082 | 4:89,735,865 | G/A | intron variant | — |
| rs3822073 | 4:89,739,624 | T/C | intron variant | — |
| rs3822072 | 4:89,741,269 | G/A | intron variant | — |
| rs28418580 | 4:89,742,244 | C/T | intron variant | — |
| rs57400569 | 4:89,752,276 | G/A | intron variant | — |
| rs4425336 | 4:89,753,225 | A/G | intron variant | — |
| rs60955950 | 4:89,756,393 | C/G | intron variant | — |
| rs7682431 | 4:89,765,661 | G/C | intron variant | — |
| rs28514678 | 4:89,768,821 | C/T | intron variant | — |
| rs2479252119 | 4:89,772,292 | C/G | — | uncertain significance |
| rs566452149 | 4:89,772,303 | T/C | — | uncertain significance |
| rs201019743 | 4:89,772,341 | G/A | — | likely benign |
| rs6830970 | 4:89,777,081 | A/G | intron variant | — |
| rs7690881 | 4:89,791,982 | A/G | — | — |
| rs28767574 | 4:89,795,609 | C/T | intron variant | — |
| rs142866806 | 4:89,795,863 | C/G | — | — |
| rs74710229 | 4:89,796,154 | T/A | — | — |
| rs17815990 | 4:89,798,892 | T/C | intron variant | — |
| rs2609255 | 4:89,811,195 | G/T | intron variant | association |
| rs13110699 | 4:89,815,695 | T/A | — | — |
| rs2446297 | 4:89,817,447 | C/G | — | — |
| rs2609259 | 4:89,837,808 | A/C | intron variant | — |
| rs9997652 | 4:89,846,749 | T/A | intron variant | — |
| rs2704589 | 4:89,848,583 | T/A | — | — |
| rs2609280 | 4:89,854,961 | A/G | intron variant | — |
| rs2609279 | 4:89,855,495 | T/C | intron variant | — |
| rs7660385 | 4:89,860,819 | T/C | intron variant | — |
| rs7682317 | 4:89,860,830 | C/T | intron variant | — |
| rs4416442 | 4:89,866,713 | T/C | intron variant | — |
| rs2869966 | 4:89,869,078 | C/A | — | — |
| rs2869967 | 4:89,869,332 | T/C | intron variant | — |
| rs1812329 | 4:89,869,918 | G/A | intron variant | — |
| rs2045517 | 4:89,870,964 | C/T | intron variant | — |
| rs7674369 | 4:89,872,176 | G/A | intron variant | — |
| rs6837671 | 4:89,873,092 | A/G | intron variant | — |
| rs1964516 | 4:89,875,909 | C/T | intron variant | — |
| rs3857043 | 4:89,882,590 | T/C | intron variant | — |
| rs3846287 | 4:89,883,112 | C/T | intron variant | — |
| rs7671167 | 4:89,883,979 | C/T | intron variant | association |
| rs2013701 | 4:89,885,086 | G/T | — | benign |
| rs4693980 | 4:89,885,988 | G/A | regulatory region variant | — |
Showing 100 of 124 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.