ClinVar Miner

List of variants in gene combination LOC101927178, PPP2R3C reported as pathogenic for spermatogenic failure

Included ClinVar conditions (116):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_017917.4(PPP2R3C):c.578T>C (p.Leu193Ser) rs1566411552 0.00001
NM_017917.4(PPP2R3C):c.1049T>C (p.Phe350Ser) rs1566684983
NM_017917.4(PPP2R3C):c.308T>C (p.Leu103Pro) rs754106837

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