ClinVar Miner

List of variants studied for spermatogenic failure by Johns Hopkins Genomics, Johns Hopkins University

Included ClinVar conditions (115):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_001206927.2(DNAH8):c.11468C>T (p.Ala3823Val) rs185283741 0.00034
NM_001206927.2(DNAH8):c.5210G>A (p.Arg1737His) rs568480936 0.00004
NM_001206927.2(DNAH8):c.3006A>T (p.Lys1002Asn) rs1268449600
NM_001206927.2(DNAH8):c.3601A>G (p.Lys1201Glu) rs1772998152
NM_001206927.2(DNAH8):c.665A>G (p.Tyr222Cys) rs753974456

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