ClinVar Miner

List of variants reported as likely benign for autism

Included ClinVar conditions (60):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_000036.3(AMPD1):c.1470C>T (p.Thr490=) rs587779371
NM_000036.3(AMPD1):c.540C>T (p.Phe180=) rs587779376
NM_000036.3(AMPD1):c.603T>A (p.Pro201=) rs587779377
NM_001329998.2(TRANK1):c.1088A>G (p.Asn363Ser)
NM_001481.3(GAS8):c.90+1487_90+1488insGCTGCCCCGCAG rs1555648296

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