ClinVar Miner

List of variants reported as benign for Spermatogenic failure 35 by Genome-Nilou Lab

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001388453.1(QRICH2):c.3713-15T>C	rs17509527	0.53425
NM_001388453.1(QRICH2):c.4748+47G>A	rs164010	0.41830
NM_001388453.1(QRICH2):c.4878G>A (p.Thr1626=)	rs347675	0.09757

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