PGAP6
post-GPI attachment to proteins 6
Summary
Predicted to enable phospholipase A2 activity. Predicted to be involved in lipid metabolic process. Located in extracellular exosome and lysosomal membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants105 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs750500500 | 16:422,012 | C/G | — | uncertain significance |
| rs372193857 | 16:422,054 | G/A | — | uncertain significance |
| rs750590444 | 16:422,067 | G/A | — | uncertain significance |
| rs143333706 | 16:422,075 | G/A | — | uncertain significance |
| rs145361083 | 16:422,085 | G/T | — | conflicting classifications of pathogenicity |
| rs2054339378 | 16:422,151 | A/G | — | uncertain significance |
| rs2548606624 | 16:422,187 | T/A | — | uncertain significance |
| rs541217650 | 16:422,202 | T/C | — | uncertain significance |
| rs747922747 | 16:422,208 | C/T | — | likely benign |
| rs150690739 | 16:422,211 | C/T | — | uncertain significance |
| rs148676257 | 16:422,261 | C/T | — | uncertain significance |
| rs139793210 | 16:422,271 | C/T | — | uncertain significance |
| rs2548607134 | 16:422,614 | C/T | — | uncertain significance |
| rs761820371 | 16:422,624 | A/T | — | uncertain significance |
| rs750242291 | 16:422,627 | A/C | — | uncertain significance |
| rs752798057 | 16:422,649 | G/A | — | uncertain significance |
| rs746218290 | 16:422,694 | T/C | — | uncertain significance |
| rs5020353 | 16:423,423 | A/C | — | — |
| rs1573734 | 16:423,619 | C/A | — | — |
| rs117037628 | 16:423,809 | A/T | — | — |
| rs28461437 | 16:423,813 | C/T | — | — |
| rs2054357001 | 16:424,024 | A/T | — | uncertain significance |
| rs567583918 | 16:424,028 | G/A | — | uncertain significance |
| rs538237652 | 16:424,050 | C/A | — | uncertain significance |
| rs755472720 | 16:424,079 | C/T | — | uncertain significance |
| rs1231155757 | 16:424,136 | C/T | — | uncertain significance |
| rs778294570 | 16:424,147 | T/C | — | uncertain significance |
| rs977410061 | 16:424,271 | A/G | — | uncertain significance |
| rs527866482 | 16:424,273 | C/T | — | uncertain significance |
| rs778779775 | 16:424,279 | A/G | — | uncertain significance |
| rs866564304 | 16:424,340 | C/T | — | uncertain significance |
| rs374985730 | 16:424,342 | C/G | — | uncertain significance |
| rs779082879 | 16:424,357 | G/A | — | uncertain significance |
| rs752273130 | 16:424,394 | G/A | — | uncertain significance |
| rs376639779 | 16:424,797 | C/T | — | uncertain significance |
| rs2054370799 | 16:425,200 | T/C | — | uncertain significance |
| rs374799437 | 16:425,224 | C/T | — | uncertain significance |
| rs147139972 | 16:425,251 | A/G | — | uncertain significance |
| rs140340682 | 16:425,351 | T/C | — | uncertain significance |
| rs780214811 | 16:425,362 | G/A | — | uncertain significance |
| rs201414656 | 16:425,378 | G/A | — | uncertain significance |
| rs202054688 | 16:425,386 | G/A | — | uncertain significance |
| rs1365342722 | 16:425,404 | G/A | — | uncertain significance |
| rs758212181 | 16:425,411 | C/T | — | likely benign |
| rs540056311 | 16:426,007 | G/C | — | — |
| rs745477438 | 16:426,147 | G/A | — | uncertain significance |
| rs151156580 | 16:426,167 | C/T | — | uncertain significance |
| rs1207215002 | 16:426,186 | T/C | — | uncertain significance |
| rs370077210 | 16:426,194 | C/T | — | uncertain significance |
| rs146617062 | 16:426,221 | G/A | — | uncertain significance |
| rs1266578538 | 16:426,224 | C/T | — | uncertain significance |
| rs141404417 | 16:426,236 | G/A | — | uncertain significance |
| rs749491361 | 16:426,269 | A/T | — | uncertain significance |
| rs145187851 | 16:426,282 | C/T | — | uncertain significance |
| rs754670088 | 16:426,290 | G/A | — | likely benign |
| rs76670391 | 16:426,296 | G/C | — | uncertain significance |
| rs1417253291 | 16:426,301 | G/A | — | likely benign |
| rs1056045918 | 16:426,319 | G/T | — | uncertain significance |
| rs965320227 | 16:426,364 | G/T | — | uncertain significance |
| rs566426734 | 16:426,392 | T/C | — | uncertain significance |
| rs568605261 | 16:426,438 | C/T | — | uncertain significance |
| rs2071916 | 16:426,476 | T/C | intron variant | — |
| rs780554251 | 16:426,549 | A/G | — | uncertain significance |
| rs2548610013 | 16:426,553 | C/T | — | uncertain significance |
| rs1028671112 | 16:426,615 | A/C | — | uncertain significance |
| rs143724021 | 16:426,651 | C/T | — | likely benign |
| rs147207812 | 16:426,670 | C/T | — | likely benign |
| rs371825117 | 16:426,685 | C/T | — | uncertain significance |
| rs149236992 | 16:426,691 | G/C | — | uncertain significance |
| rs1305775935 | 16:426,695 | G/T | — | uncertain significance |
| rs774975652 | 16:426,720 | A/G | — | uncertain significance |
| rs774539748 | 16:427,058 | A/G | — | uncertain significance |
| rs781063232 | 16:427,091 | A/G | — | uncertain significance |
| rs202157156 | 16:427,113 | G/A | — | uncertain significance |
| rs202229020 | 16:427,115 | G/A | — | uncertain significance |
| rs145211537 | 16:427,147 | A/C | — | uncertain significance |
| rs531585905 | 16:427,386 | C/T | — | uncertain significance |
| rs371688676 | 16:427,393 | C/A | — | uncertain significance |
| rs1441140767 | 16:427,407 | G/C | — | uncertain significance |
| rs781154521 | 16:427,416 | C/T | — | uncertain significance |
| rs765157410 | 16:427,442 | G/A | — | uncertain significance |
| rs754371790 | 16:427,458 | C/T | — | likely benign |
| rs989762554 | 16:427,468 | G/C | — | uncertain significance |
| rs11248931 | 16:427,479 | T/G | missense variant | — |
| rs377646422 | 16:427,490 | G/A | — | likely benign |
| rs373171599 | 16:427,523 | G/C | — | uncertain significance |
| rs548358622 | 16:427,672 | C/T | — | uncertain significance |
| rs1197072875 | 16:427,744 | C/G | — | uncertain significance |
| rs199670311 | 16:427,758 | C/T | missense variant | — |
| rs757017387 | 16:427,759 | G/A | — | uncertain significance |
| rs780259764 | 16:427,764 | C/T | — | likely benign |
| rs143766173 | 16:427,765 | G/A | — | uncertain significance |
| rs868534529 | 16:427,812 | G/A | — | uncertain significance |
| rs61261356 | 16:427,925 | T/G | — | — |
| rs56990244 | 16:427,999 | C/A | — | — |
| rs577420328 | 16:428,086 | C/T | — | — |
| rs12921174 | 16:430,304 | T/A | — | — |
| rs1215433854 | 16:431,728 | C/T | — | uncertain significance |
| rs1277968041 | 16:431,731 | G/A | — | uncertain significance |
| rs1033939884 | 16:431,742 | G/A | — | uncertain significance |
Showing 100 of 105 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.