C0546837[trait identifier] AND "Center for Genomics, Ann and Robert H. - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 626031	NM_003242.6(TGFBR2):c.413G>A (p.Cys138Tyr)	TGFBR2 (C163Y +3 more)	Single nucleotide variant (missense variant)	Malignant tumor of esophagus +2 more	GUncertain significance
Select item 923453	NM_003242.6(TGFBR2):c.505G>C (p.Gly169Arg)	TGFBR2 (G169R +8 more)	Single nucleotide variant (missense variant)	not specified +4 more	GUncertain significance
Select item 36859	NM_003242.6(TGFBR2):c.1119G>A (p.Met373Ile)	TGFBR2 (M373I +8 more)	Single nucleotide variant (missense variant)	Colorectal cancer, hereditary nonpolyposis, type 6 +9 more	GBenign/Likely benign
Select item 44651	NM_003242.6(TGFBR2):c.1159G>A (p.Val387Met)	TGFBR2 (V387M +8 more)	Single nucleotide variant (missense variant)	Loeys-Dietz syndrome 2 +9 more	GConflicting classifications of pathogenicity
Select item 626183	NM_003242.6(TGFBR2):c.1682G>C (p.Gly561Ala)	TGFBR2 (G586A +10 more)	Single nucleotide variant (missense variant)	Malignant tumor of esophagus +2 more	GUncertain significance
Select item 626053	NM_016373.4(WWOX):c.517-108243C>T	WWOX	Single nucleotide variant (synonymous variant +2 more)	Autosomal recessive spinocerebellar ataxia 12 +2 more	GUncertain significance

ClinVar