Related gene-specific medical variations for Gene (Select 2040) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2375513	NM_004099.6(STOM):c.39G>C (p.Gln13His)	LOC102723324, STOM (Q13H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1163314	NM_004099.6(STOM):c.2T>C (p.Met1Thr)	LOC102723324, STOM (M1T)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 815292	GRCh37/hg19 9q33.2(chr9:124107297-124159211)x1	STOM	Copy number loss	not provided	GUncertain significance

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