Related gene-specific medical variations for Gene (Select 4008) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290990	NM_005358.5(LMO7):c.102G>T (p.Arg34Ser)	LMO7, LMO7-AS1 (R34S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119361	NM_005358.5(LMO7):c.136G>C (p.Gly46Arg)	LMO7, LMO7-AS1 (G46R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2628008	NM_001306080.2(LMO7):c.1883G>C (p.Arg628Thr)	LMO7 (R301T +3 more)	Single nucleotide variant (missense variant +1 more)	Bladder exstrophy-epispadias-cloacal extrophy complex	GUncertain significance
Select item 2602102	NM_005358.5(LMO7):c.156C>A (p.Asp52Glu)	LMO7, LMO7-AS1 (D52E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2537888	NM_005358.5(LMO7):c.169A>G (p.Lys57Glu)	LMO7, LMO7-AS1 (K57E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523858	NM_005358.5(LMO7):c.179T>C (p.Ile60Thr)	LMO7, LMO7-AS1 (I60T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490337	NM_005358.5(LMO7):c.214A>T (p.Ile72Phe)	LMO7, LMO7-AS1 (I72F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410517	NM_005358.5(LMO7):c.53A>G (p.Tyr18Cys)	LMO7, LMO7-AS1 (Y18C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211229	NM_005358.5(LMO7):c.112T>C (p.Cys38Arg)	LMO7, LMO7-AS1 (C38R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance