Related gene-specific medical variations for Gene (Select 8846) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3286797	NM_006020.3(ALKBH1):c.31G>A (p.Val11Met)	ALKBH1, LOC130056190 (V11M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510918	NM_006020.3(ALKBH1):c.22G>T (p.Val8Leu)	ALKBH1, LOC130056190 (V8L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance