Related gene-specific medical variations for Gene (Select 130060581) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3082057	NM_144683.4(DHRS13):c.83G>A (p.Cys28Tyr)	DHRS13, LOC130060581 (C28Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2647604	NM_144683.4(DHRS13):c.129C>A (p.Gly43=)	DHRS13, LOC130060581	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2334516	NM_144683.4(DHRS13):c.64C>G (p.Leu22Val)	DHRS13, LOC130060581 (L22V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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