ClinVar for MedGen (Select 436866) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2247899	NM_005904.4(SMAD7):c.166G>A (p.Gly56Ser)	SMAD7 (G56S)	Single nucleotide variant (missense variant)	Colorectal cancer, susceptibility to, 3 +1 more	GUncertain significance
Select item 6725	NM_005904.4(SMAD7):c.743-5183=	SMAD7	Single nucleotide variant (intron variant)	Colorectal cancer, susceptibility to, 3	Grisk factor