Related gene-specific medical variations for Gene (Select 10099) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685525	GRCh37/hg19 15q24.3(chr15:77334067-77386121)x1	TSPAN3	Copy number loss	not provided	GUncertain significance
Select item 2604987	NM_005724.6(TSPAN3):c.50A>G (p.Asn17Ser)	LOC130057655, TSPAN3 (N17S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2303502	NM_005724.6(TSPAN3):c.20C>T (p.Thr7Ile)	LOC130057655, TSPAN3 (T7I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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