Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72551363
rs72551363
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1720861
Disease:
Familial Partial Lipodystrophy, Type 3
A 0.800 CausalMutation CLINVAR
dbSNP: rs72551364
rs72551364
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1720861
Disease:
Familial Partial Lipodystrophy, Type 3
T 0.800 CausalMutation CLINVAR
dbSNP: rs121909242
rs121909242
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C0007102
Disease:
Malignant tumor of colon
0.700 GeneticVariation UNIPROT
dbSNP: rs121909242
rs121909242
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C0009402
Disease:
Colorectal Carcinoma
C 0.700 CausalMutation CLINVAR
dbSNP: rs121909243
rs121909243
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C0009402
Disease:
Colorectal Carcinoma
T 0.700 CausalMutation CLINVAR
dbSNP: rs121909244
rs121909244
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1720861
Disease:
Familial Partial Lipodystrophy, Type 3
T 0.700 CausalMutation CLINVAR
dbSNP: rs121909245
rs121909245
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1720861
Disease:
Familial Partial Lipodystrophy, Type 3
A 0.700 CausalMutation CLINVAR
dbSNP: rs121909246
rs121909246
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1720861
Disease:
Familial Partial Lipodystrophy, Type 3
T 0.700 CausalMutation CLINVAR
dbSNP: rs1378972597
rs1378972597
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1720861
Disease:
Familial Partial Lipodystrophy, Type 3
C 0.700 GeneticVariation CLINVAR
dbSNP: rs148195788
rs148195788
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1720861
Disease:
Familial Partial Lipodystrophy, Type 3
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1553638903
rs1553638903
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1553638909
rs1553638909
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1553643326
rs1553643326
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1720861
Disease:
Familial Partial Lipodystrophy, Type 3
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1553647989
rs1553647989
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1720861
Disease:
Familial Partial Lipodystrophy, Type 3
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1553650477
rs1553650477
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1720861
Disease:
Familial Partial Lipodystrophy, Type 3
T 0.700 CausalMutation CLINVAR
dbSNP: rs1553653993
rs1553653993
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1720861
Disease:
Familial Partial Lipodystrophy, Type 3
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1800571
rs1800571
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C0028756
Disease:
Obesity, Morbid
A 0.700 CausalMutation CLINVAR
dbSNP: rs1800571
rs1800571
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C0028754
Disease:
Obesity
0.700 GeneticVariation UNIPROT
dbSNP: rs1805192
rs1805192
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1832251
Disease:
BODY MASS INDEX, MODIFIER OF
G 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs1805192
rs1805192
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1832250
Disease:
OBESITY, MODIFIER OF
G 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs1805192
rs1805192
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C4016735
Disease:
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF
G 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs1805192
rs1805192
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C1832253
Disease:
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
G 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs28936407
rs28936407
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C0007102
Disease:
Malignant tumor of colon
0.700 GeneticVariation UNIPROT
dbSNP: rs28936407
rs28936407
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C0009402
Disease:
Colorectal Carcinoma
A 0.700 CausalMutation CLINVAR
dbSNP: rs587776687
rs587776687
Entrez Id: 5468
Gene Symbol: PPARG
PPARG
CUI: C0009402
Disease:
Colorectal Carcinoma
C 0.700 CausalMutation CLINVAR