List of variants reported as pathogenic for Spermatogenic failure 38 by OMIM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_032131.6(ARMC2):c.1023+1G>A	rs1562372417
NM_032131.6(ARMC2):c.1284_1288del (p.Lys428fs)	rs1562381747
NM_032131.6(ARMC2):c.2279T>A (p.Ile760Asn)	rs1562435988
NM_032131.6(ARMC2):c.2353_2354del (p.Leu785fs)	rs1562436860
NM_032131.6(ARMC2):c.421C>T (p.Gln141Ter)	rs1562332833

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