List of variants in gene QRICH2 studied for Spermatogenic failure 35

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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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	0.41462
NM_001388453.1(QRICH2):c.4878G>A (p.Thr1626=)	rs347675	0.09757
NM_001388453.1(QRICH2):c.3535C>T (p.Arg1179Ter)	rs777214459	0.00003
NM_001388453.1(QRICH2):c.3999C>G (p.Tyr1333Ter)	rs934388592	0.00001
NM_001388453.1(QRICH2):c.4306G>A (p.Val1436Met)
NM_001388453.1(QRICH2):c.5112C>G (p.Tyr1704Ter)	rs770382841
NM_001388453.1(QRICH2):c.690G>A (p.Trp230Ter)	rs1567790522

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