Related gene-specific medical variations for Gene (Select 6801) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3171647	NM_003162.4(STRN):c.98C>G (p.Ala33Gly)	LOC129933482, STRN (A33G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171642	NM_003162.4(STRN):c.19C>G (p.Pro7Ala)	LOC129933482, STRN (P7A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569553	NM_003162.4(STRN):c.55G>A (p.Gly19Ser)	LOC129933482, STRN (G19S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510899	NM_003162.4(STRN):c.13G>A (p.Ala5Thr)	LOC129933482, STRN (A5T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492936	NM_003162.4(STRN):c.109G>A (p.Ala37Thr)	LOC129933482, STRN (A37T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290114	NM_003162.4(STRN):c.20C>T (p.Pro7Leu)	LOC129933482, STRN (P7L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281350	NM_003162.4(STRN):c.198G>T (p.Glu66Asp)	LOC129933482, STRN (E66D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219447	NM_003162.4(STRN):c.13G>C (p.Ala5Pro)	LOC129933482, STRN (A5P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar