ClinVar Miner

List of variants in gene GK reported as likely pathogenic by GeneDx

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_001205019.2(GK):c.1232G>A (p.Arg411Gln)	rs2519351408
NM_001205019.2(GK):c.385del (p.Arg129fs)	rs1601910946

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