List of variants in gene GCDH reported as likely pathogenic by Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000159.4(GCDH):c.1207C>T (p.His403Tyr)	rs1599619080
NM_000159.4(GCDH):c.528C>G (p.Cys176Trp)	rs756345321
NM_000159.4(GCDH):c.881G>C (p.Arg294Pro)	rs775606471

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