C0268595[trait identifier] AND "Institute of Human Genetics Munich, Kl - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 188789	NM_000159.4(GCDH):c.482G>A (p.Arg161Gln)	GCDH (R161Q)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 2086	NM_000159.4(GCDH):c.1093G>A (p.Glu365Lys)	GCDH (E365K)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic
Select item 193798	NM_000159.4(GCDH):c.1213A>G (p.Met405Val)	GCDH (M405V)	Single nucleotide variant (missense variant +1 more)	GCDH-related condition +2 more	GPathogenic/Likely pathogenic

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