ClinVar Miner

List of variants in gene GRK1 reported as likely pathogenic by Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002929.3(GRK1):c.1139T>A (p.Val380Asp)	rs777094000	0.00004
NM_002929.3(GRK1):c.1312C>T (p.Arg438Cys)	rs765070399

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