Related gene-specific medical variations for Gene (Select 389816) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2659812	NM_001013653.3(LRRC26):c.444C>T (p.Leu148=)	LOC130003088, LRRC26	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2604404	NM_001013653.3(LRRC26):c.598G>A (p.Gly200Ser)	LOC130003088, LRRC26 (G200S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2540583	NM_001013653.3(LRRC26):c.500C>G (p.Pro167Arg)	LOC130003088, LRRC26 (P167R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2525645	NM_001013653.3(LRRC26):c.641C>G (p.Ala214Gly)	LOC130003088, LRRC26 (A214G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2514608	NM_001013653.3(LRRC26):c.469C>T (p.Arg157Cys)	LOC130003088, LRRC26 (R157C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460542	NM_001013653.3(LRRC26):c.404C>T (p.Ala135Val)	LOC130003088, LRRC26 (A135V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2396148	NM_001013653.3(LRRC26):c.193G>A (p.Val65Met)	LOC130003089, LRRC26 (V65M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2370169	NM_001013653.3(LRRC26):c.616G>T (p.Gly206Trp)	LOC130003088, LRRC26 (G206W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2347838	NM_001013653.3(LRRC26):c.595C>T (p.Arg199Cys)	LOC130003088, LRRC26 (R199C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2345095	NM_001013653.3(LRRC26):c.632C>T (p.Pro211Leu)	LOC130003088, LRRC26 (P211L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2334861	NM_001013653.3(LRRC26):c.715C>T (p.Leu239Phe)	LOC130003088, LRRC26 (L239F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2261066	NM_001013653.3(LRRC26):c.662T>G (p.Leu221Arg)	LOC130003088, LRRC26 (L221R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2256074	NM_001013653.3(LRRC26):c.208A>C (p.Ser70Arg)	LOC130003089, LRRC26 (S70R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2255817	NM_001013653.3(LRRC26):c.647T>G (p.Leu216Arg)	LOC130003088, LRRC26 (L216R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2209342	NM_001013653.3(LRRC26):c.566G>C (p.Arg189Pro)	LOC130003088, LRRC26 (R189P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2204611	NM_001013653.3(LRRC26):c.541G>A (p.Ala181Thr)	LOC130003088, LRRC26 (A181T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 776483	NM_001013653.3(LRRC26):c.724C>G (p.Leu242Val)	LOC130003088, LRRC26 (L242V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 760213	NM_001013653.3(LRRC26):c.807G>T (p.Gly269=)	LOC130003088, LRRC26	Single nucleotide variant (synonymous variant)	not provided	GLikely benign