DAAM2
dishevelled associated activator of morphogenesis 2
Summary
Predicted to enable actin binding activity and small GTPase binding activity. Involved in several processes, including podocyte cell migration; regulation of actin filament polymerization; and regulation of filopodium assembly. Located in extracellular exosome. Implicated in familial nephrotic syndrome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants137 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs564451966 | 6:39,779,712 | A/G | — | — |
| rs2395730 | 6:39,784,365 | C/A | intron variant | — |
| rs6937133 | 6:39,800,014 | A/T | — | — |
| rs551879834 | 6:39,818,455 | G/C | — | — |
| rs2504106 | 6:39,822,119 | A/G | intron variant | — |
| rs775379327 | 6:39,824,089 | G/T | — | uncertain significance |
| rs527543903 | 6:39,824,098 | G/A | — | uncertain significance |
| rs11965120 | 6:39,824,105 | T/C | — | benign |
| rs376650953 | 6:39,824,129 | C/T | — | likely benign |
| rs199767843 | 6:39,824,130 | G/A | — | benign |
| rs745986379 | 6:39,824,160 | C/T | — | uncertain significance |
| rs370984960 | 6:39,824,207 | G/A | — | likely benign |
| rs535365178 | 6:39,824,210 | C/T | — | likely benign |
| rs370116070 | 6:39,828,743 | T/C | — | uncertain significance |
| rs370112679 | 6:39,828,755 | C/A | — | uncertain significance |
| rs1582695874 | 6:39,832,222 | C/T | — | uncertain significance |
| rs376069544 | 6:39,832,263 | C/T | — | uncertain significance |
| rs6919807 | 6:39,832,264 | G/A | — | benign |
| rs1391253919 | 6:39,832,783 | G/C | — | pathogenic |
| rs1217115548 | 6:39,832,834 | C/T | — | uncertain significance |
| rs543612445 | 6:39,832,835 | G/A | — | uncertain significance |
| rs2504093 | 6:39,832,964 | T/C | regulatory region variant | — |
| rs73734938 | 6:39,835,276 | T/C | — | benign |
| rs1486079417 | 6:39,835,363 | G/C | — | uncertain significance |
| rs367610796 | 6:39,835,371 | C/T | — | uncertain significance |
| rs200589550 | 6:39,835,372 | G/A | — | benign |
| rs115708591 | 6:39,835,449 | C/T | — | uncertain significance |
| rs375083979 | 6:39,835,482 | C/G | — | uncertain significance |
| rs114233535 | 6:39,835,590 | G/C | — | benign |
| rs775432314 | 6:39,835,597 | C/T | — | uncertain significance |
| rs575251556 | 6:39,835,611 | C/T | — | uncertain significance |
| rs34941067 | 6:39,836,610 | C/T | — | benign |
| rs925350528 | 6:39,836,620 | C/G | — | uncertain significance |
| rs199545289 | 6:39,836,633 | G/A | — | uncertain significance |
| rs551076398 | 6:39,836,672 | C/T | — | likely benign |
| rs2481755356 | 6:39,838,197 | C/T | — | uncertain significance |
| rs531101009 | 6:39,839,297 | C/T | — | likely benign |
| rs371806282 | 6:39,839,307 | C/T | — | uncertain significance |
| rs200668867 | 6:39,839,308 | G/A | — | pathogenic |
| rs1027404379 | 6:39,839,346 | A/G | — | uncertain significance |
| rs551041219 | 6:39,843,117 | G/C | — | uncertain significance |
| rs370084680 | 6:39,843,146 | G/A | — | likely benign |
| rs561512895 | 6:39,843,153 | A/G | — | uncertain significance |
| rs201940753 | 6:39,843,179 | T/G | — | uncertain significance |
| rs1435790953 | 6:39,843,180 | G/A | — | uncertain significance |
| rs2481812045 | 6:39,843,198 | G/C | — | uncertain significance |
| rs757546813 | 6:39,843,237 | G/A | — | uncertain significance |
| rs1764951663 | 6:39,846,010 | C/T | — | pathogenic |
| rs183543237 | 6:39,846,016 | C/G | — | likely benign |
| rs373715976 | 6:39,846,187 | G/A | — | uncertain significance |
| rs1427897271 | 6:39,846,216 | A/G | — | uncertain significance |
| rs192352327 | 6:39,846,264 | C/T | — | uncertain significance |
| rs369945548 | 6:39,846,321 | G/A | — | uncertain significance |
| rs889852609 | 6:39,846,967 | C/T | — | uncertain significance |
| rs909026840 | 6:39,846,972 | C/T | — | uncertain significance |
| rs1035310700 | 6:39,846,989 | C/T | — | likely benign |
| rs1765009009 | 6:39,847,036 | C/T | — | uncertain significance |
| rs753628535 | 6:39,847,051 | C/T | — | uncertain significance |
| rs201570348 | 6:39,847,072 | C/T | — | likely benign |
| rs775891415 | 6:39,847,076 | A/C | — | likely benign |
| rs199956358 | 6:39,847,126 | C/T | — | benign |
| rs2481856192 | 6:39,847,143 | C/T | — | likely benign |
| rs150676991 | 6:39,847,153 | C/A | — | uncertain significance |
| rs766614312 | 6:39,847,197 | C/T | — | likely benign |
| rs181701991 | 6:39,847,198 | G/C | — | uncertain significance |
| rs139876341 | 6:39,847,207 | A/G | — | benign |
| rs1765023864 | 6:39,847,218 | C/T | — | uncertain significance |
| rs2481858103 | 6:39,847,260 | A/G | — | likely benign |
| rs34699846 | 6:39,851,742 | G/A | — | benign |
| rs182055289 | 6:39,851,791 | G/T | — | likely benign |
| rs3003929 | 6:39,851,818 | G/A | — | benign |
| rs35383047 | 6:39,855,288 | C/A | — | benign |
| rs370740545 | 6:39,855,334 | C/T | — | uncertain significance |
| rs373552829 | 6:39,856,481 | G/A | — | uncertain significance |
| rs61757199 | 6:39,856,489 | A/G | — | uncertain significance |
| rs1207427310 | 6:39,856,494 | G/C | — | uncertain significance |
| rs372115052 | 6:39,856,534 | G/C | — | uncertain significance |
| rs1309933460 | 6:39,859,174 | G/A | — | uncertain significance |
| rs767650659 | 6:39,859,193 | G/A | — | uncertain significance |
| rs200287086 | 6:39,859,415 | A/G | — | likely benign |
| rs570413956 | 6:39,859,436 | A/G | — | uncertain significance |
| rs2481998892 | 6:39,859,480 | G/C | — | uncertain significance |
| rs201229313 | 6:39,859,484 | A/C | — | likely benign |
| rs368625687 | 6:39,864,578 | C/T | — | likely benign |
| rs368057856 | 6:39,864,618 | G/A | — | uncertain significance |
| rs200279541 | 6:39,864,626 | C/T | — | uncertain significance |
| rs766125641 | 6:39,864,692 | G/A | — | uncertain significance |
| rs949037582 | 6:39,864,719 | C/T | — | uncertain significance |
| rs3008815 | 6:39,864,730 | C/T | — | benign |
| rs2482082123 | 6:39,864,737 | A/G | — | uncertain significance |
| rs116568611 | 6:39,864,764 | C/T | — | benign |
| rs199666036 | 6:39,864,952 | A/C | — | uncertain significance |
| rs61748650 | 6:39,865,007 | T/C | — | likely benign |
| rs761116581 | 6:39,865,018 | C/G | — | uncertain significance |
| rs2482089288 | 6:39,865,039 | C/T | — | uncertain significance |
| rs3004067 | 6:39,865,047 | T/C | — | benign |
| rs61748651 | 6:39,866,692 | G/C | — | uncertain significance |
| rs780925746 | 6:39,866,695 | C/T | — | likely benign |
| rs185163538 | 6:39,866,711 | G/C | — | uncertain significance |
| rs750321033 | 6:39,867,855 | G/A | — | likely benign |
Showing 100 of 137 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.