SMAD6, SMAD family member 6, 4091

N. diseases: 93; N. variants: 26
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907283
rs387907283
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C3542024
Disease:
AORTIC VALVE DISEASE 2
0.800 GeneticVariation UNIPROT
dbSNP: rs387907283
rs387907283
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C3542024
Disease:
AORTIC VALVE DISEASE 2
T 0.800 CausalMutation CLINVAR
dbSNP: rs387907284
rs387907284
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C3542024
Disease:
AORTIC VALVE DISEASE 2
T 0.800 CausalMutation CLINVAR
dbSNP: rs387907284
rs387907284
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C3542024
Disease:
AORTIC VALVE DISEASE 2
0.800 GeneticVariation UNIPROT
dbSNP: rs12594720
rs12594720
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C0007102
Disease:
Malignant tumor of colon
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs12594720
rs12594720
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C0009404
Disease:
Colorectal Neoplasms
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs12594720
rs12594720
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs12594720
rs12594720
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs12594720
rs12594720
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs12594720
rs12594720
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C0346629
Disease:
Malignant neoplasm of large intestine
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs12594720
rs12594720
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C0009402
Disease:
Colorectal Carcinoma
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs12594720
rs12594720
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs12594720
rs12594720
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C1302401
Disease:
Adenoma of large intestine
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs12594720
rs12594720
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C1319315
Disease:
Adenocarcinoma of large intestine
C 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs1440372
rs1440372
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C0205682
Disease:
Waist-Hip Ratio
T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs1440374
rs1440374
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C0042834
Disease:
Vital capacity
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1866745
rs1866745
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C0007286
Disease:
Carpal Tunnel Syndrome
A 0.700 GeneticVariation GWASCAT A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome. 30833571 2019
dbSNP: rs2119260
rs2119260
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C0205682
Disease:
Waist-Hip Ratio
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3809570
rs3809570
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C0424678
Disease:
Lean body mass
0.700 GeneticVariation GWASCAT Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. 30593698 2019
dbSNP: rs4776316
rs4776316
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs4776316
rs4776316
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C0009402
Disease:
Colorectal Carcinoma
A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs4776316
rs4776316
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs4776316
rs4776316
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs4776316
rs4776316
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C0007102
Disease:
Malignant tumor of colon
A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs4776316
rs4776316
Entrez Id: 4091
Gene Symbol: SMAD6
SMAD6
CUI: C1319315
Disease:
Adenocarcinoma of large intestine
A 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019