List of variants in gene GRHPR reported as likely benign for GRHPR-related disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_012203.2(GRHPR):c.286C>T (p.Arg96Cys)	rs78920863	0.00130
NM_012203.2(GRHPR):c.-3C>T	rs200847843	0.00003
NM_012203.2(GRHPR):c.252C>A (p.Gly84=)	rs139595138	0.00003
NM_012203.2(GRHPR):c.-4G>A	rs201826196	0.00001

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