Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34833812
rs34833812
Entrez Id: 7048
Gene Symbol: TGFBR2
TGFBR2
CUI: C1860896
Disease:
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
0.800 GeneticVariation UNIPROT HNPCC associated with germline mutation in the TGF-beta type II receptor gene. 9590282 1998
dbSNP: rs34833812
rs34833812
Entrez Id: 7048
Gene Symbol: TGFBR2
TGFBR2
CUI: C1860896
Disease:
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
T 0.800 CausalMutation CLINVAR
dbSNP: rs104893815
rs104893815
Entrez Id: 7048
Gene Symbol: TGFBR2
TGFBR2
CUI: C1860896
Disease:
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
A 0.700 CausalMutation CLINVAR
dbSNP: rs104893819
rs104893819
Entrez Id: 7048
Gene Symbol: TGFBR2
TGFBR2
CUI: C1860896
Disease:
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
T 0.700 CausalMutation CLINVAR
dbSNP: rs587776769
rs587776769
Entrez Id: 7048
Gene Symbol: TGFBR2
TGFBR2
CUI: C1860896
Disease:
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
AGT 0.700 CausalMutation CLINVAR