Related gene-specific medical variations for Gene (Select 118932) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290833	NM_001128215.1(LIPM):c.1196T>C (p.Met399Thr)	ANKRD22, LIPM (M399T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2621064	NM_001128215.1(LIPM):c.1101G>A (p.Met367Ile)	ANKRD22, LIPM (M367I)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2458010	NM_001128215.1(LIPM):c.1250G>C (p.Gly417Ala)	ANKRD22, LIPM (G417A)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2377839	NM_001128215.1(LIPM):c.1253G>A (p.Arg418Gln)	ANKRD22, LIPM (R418Q)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance

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