Related gene-specific medical variations for Gene (Select 7097) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2250336	NM_173662.4(RNF175):c.944T>C (p.Ile315Thr)	RNF175, TLR2 (I315T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 111268	NM_001318789.2(TLR2):c.265A>G (p.Asn89Asp)	TLR2 (N89D)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 6664	NG_016229.2:g.23486GT[26_43]	TLR2	Microsatellite	Colorectal cancer, susceptibility to	Grisk factor

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