SEMA5A
semaphorin 5A
Summary
This gene belongs to the semaphorin gene family that encodes membrane proteins containing a semaphorin domain and several thrombospondin type-1 repeats. Members of this family are involved in axonal guidance during neural development. This gene has been implicated as an autism susceptibility gene.[provided by RefSeq, Jan 2010]
Known Variants153 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs759802757 | 5:9,043,077 | G/C | — | uncertain significance |
| rs1579289990 | 5:9,043,105 | G/A | — | likely benign |
| rs1579290031 | 5:9,043,136 | A/G | — | likely benign |
| rs150116452 | 5:9,044,500 | C/T | — | likely benign |
| rs139191700 | 5:9,044,551 | G/A | — | likely benign |
| rs368954618 | 5:9,044,566 | G/A | — | likely benign |
| rs138582608 | 5:9,044,582 | G/A | — | likely benign |
| rs147519596 | 5:9,044,587 | G/A | — | benign |
| rs138316526 | 5:9,044,606 | C/T | — | benign |
| rs762391468 | 5:9,044,611 | G/A | — | likely benign |
| rs376502162 | 5:9,044,625 | C/T | — | uncertain significance |
| rs201531529 | 5:9,044,646 | C/T | — | uncertain significance |
| rs11741172 | 5:9,044,647 | A/G | — | benign |
| rs386352358 | 5:9,044,662 | C/G | — | uncertain significance |
| rs529504980 | 5:9,044,670 | C/G | — | uncertain significance |
| rs1057015686 | 5:9,050,524 | C/T | — | uncertain significance |
| rs201581372 | 5:9,050,543 | C/T | — | uncertain significance |
| rs777578380 | 5:9,050,546 | T/C | — | uncertain significance |
| rs34563995 | 5:9,050,549 | T/C | — | benign |
| rs141409163 | 5:9,050,577 | A/G | — | likely benign |
| rs781047921 | 5:9,051,975 | C/T | — | likely benign |
| rs140105544 | 5:9,051,977 | G/C | — | benign |
| rs1291334324 | 5:9,052,011 | C/T | — | uncertain significance |
| rs145965659 | 5:9,052,013 | C/T | — | benign |
| rs371373696 | 5:9,052,017 | C/T | — | uncertain significance |
| rs139882587 | 5:9,052,036 | C/T | — | uncertain significance |
| rs754602220 | 5:9,052,072 | A/G | — | uncertain significance |
| rs780818611 | 5:9,052,075 | G/T | — | uncertain significance |
| rs199614651 | 5:9,052,081 | C/T | — | uncertain significance |
| rs144048830 | 5:9,052,127 | C/T | — | benign |
| rs199709959 | 5:9,052,140 | T/C | — | uncertain significance |
| rs373427977 | 5:9,054,193 | G/A | — | likely benign |
| rs142342147 | 5:9,054,212 | C/T | — | likely benign |
| rs79460840 | 5:9,054,269 | C/T | — | benign |
| rs746993347 | 5:9,054,289 | A/T | — | uncertain significance |
| rs201560724 | 5:9,054,293 | G/A | — | likely benign |
| rs762572657 | 5:9,054,309 | C/T | — | uncertain significance |
| rs146447120 | 5:9,054,313 | C/T | — | conflicting classifications of pathogenicity |
| rs754390056 | 5:9,054,317 | G/A | — | likely benign |
| rs200432205 | 5:9,054,377 | G/A | — | likely benign |
| rs777278438 | 5:9,063,051 | A/G | — | likely benign |
| rs759201612 | 5:9,063,074 | C/T | — | uncertain significance |
| rs144973280 | 5:9,063,124 | C/T | — | uncertain significance |
| rs1436765433 | 5:9,063,125 | G/A | — | uncertain significance |
| rs77204181 | 5:9,063,141 | C/T | — | benign |
| rs116183783 | 5:9,063,144 | C/T | — | benign |
| rs190230732 | 5:9,063,177 | G/A | — | likely benign |
| rs142331748 | 5:9,063,189 | C/A | — | likely benign |
| rs139823470 | 5:9,066,560 | C/A | — | likely benign |
| rs369672845 | 5:9,066,576 | C/A | — | uncertain significance |
| rs1131691745 | 5:9,066,592 | C/T | — | uncertain significance |
| rs142642861 | 5:9,066,618 | A/G | — | likely benign |
| rs932619445 | 5:9,066,638 | T/C | — | uncertain significance |
| rs151007766 | 5:9,066,665 | C/T | — | uncertain significance |
| rs1474483753 | 5:9,108,277 | C/T | — | uncertain significance |
| rs147869499 | 5:9,108,296 | G/A | — | uncertain significance |
| rs149012151 | 5:9,108,321 | T/C | — | benign |
| rs149188938 | 5:9,108,354 | T/A | — | benign |
| rs2477621626 | 5:9,108,361 | A/G | — | uncertain significance |
| rs2477621657 | 5:9,108,362 | A/C | — | uncertain significance |
| rs751808284 | 5:9,108,363 | C/T | — | uncertain significance |
| rs778638409 | 5:9,108,391 | T/C | — | uncertain significance |
| rs777269591 | 5:9,119,148 | G/A | — | likely benign |
| rs143358731 | 5:9,119,176 | C/T | — | uncertain significance |
| rs2477700016 | 5:9,119,177 | G/A | — | uncertain significance |
| rs1341714125 | 5:9,119,219 | G/A | — | uncertain significance |
| rs2477727504 | 5:9,122,763 | C/A | — | uncertain significance |
| rs142217030 | 5:9,122,782 | G/A | — | benign |
| rs2477728441 | 5:9,122,807 | T/G | — | uncertain significance |
| rs199595571 | 5:9,122,838 | C/T | — | uncertain significance |
| rs138508684 | 5:9,122,839 | G/A | — | benign |
| rs771022139 | 5:9,122,847 | G/A | — | uncertain significance |
| rs763769951 | 5:9,122,874 | C/T | — | uncertain significance |
| rs144932049 | 5:9,122,878 | G/T | — | benign |
| rs17238053 | 5:9,122,890 | C/A | — | benign |
| rs2477730961 | 5:9,122,919 | C/T | — | uncertain significance |
| rs144473454 | 5:9,136,617 | G/A | — | uncertain significance |
| rs201206342 | 5:9,136,622 | C/T | — | likely benign |
| rs202102793 | 5:9,136,623 | G/A | — | uncertain significance |
| rs17238609 | 5:9,136,646 | C/G | — | benign |
| rs139868902 | 5:9,136,647 | G/A | — | uncertain significance |
| rs151058285 | 5:9,136,662 | T/C | — | uncertain significance |
| rs2477845372 | 5:9,136,674 | G/A | — | uncertain significance |
| rs141004409 | 5:9,136,725 | A/G | — | uncertain significance |
| rs146836181 | 5:9,154,650 | C/T | — | benign |
| rs1806151 | 5:9,154,659 | C/G | — | benign |
| rs780008482 | 5:9,154,717 | C/T | — | uncertain significance |
| rs1742854078 | 5:9,154,735 | T/A | — | uncertain significance |
| rs138503384 | 5:9,154,774 | A/T | — | uncertain significance |
| rs138343991 | 5:9,154,783 | C/T | — | uncertain significance |
| rs200292451 | 5:9,154,784 | G/A | — | uncertain significance |
| rs1806150 | 5:9,154,803 | G/A | — | benign |
| rs201120126 | 5:9,190,403 | C/T | — | uncertain significance |
| rs769949871 | 5:9,190,427 | C/T | — | uncertain significance |
| rs773209160 | 5:9,190,430 | C/T | — | uncertain significance |
| rs143464187 | 5:9,190,439 | C/T | — | benign |
| rs1745039779 | 5:9,190,529 | C/A | — | uncertain significance |
| rs138777488 | 5:9,190,544 | C/T | — | uncertain significance |
| rs150952790 | 5:9,190,545 | G/A | — | benign |
| rs750122183 | 5:9,190,557 | G/A | — | likely benign |
Showing 100 of 153 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.