ClinVar Miner

List of variants studied for Spermatogenic failure 25 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001350162.2(TEX15):c.1261G>A (p.Gly421Ser)	rs951031727	0.00002
NM_001350162.2(TEX15):c.6869_6872del (p.Lys2290fs)	rs1224137237

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