rs12427600
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
C
0.700
GeneticVariation
GWASCAT
Association analyses identify 31 new risk loci for colorectal cancer susceptibility.
31089142
2019
rs12427600
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Adenocarcinoma of large intestine
C
0.700
GeneticVariation
GWASCAT
Association analyses identify 31 new risk loci for colorectal cancer susceptibility.
31089142
2019
rs12427600
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Malignant tumor of colon
C
0.700
GeneticVariation
GWASCAT
Association analyses identify 31 new risk loci for colorectal cancer susceptibility.
31089142
2019
rs12427600
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
C
0.700
GeneticVariation
GWASCAT
Association analyses identify 31 new risk loci for colorectal cancer susceptibility.
31089142
2019
rs12427600
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
C
0.700
GeneticVariation
GWASCAT
Association analyses identify 31 new risk loci for colorectal cancer susceptibility.
31089142
2019
rs12427600
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Colorectal Neoplasms
C
0.700
GeneticVariation
GWASCAT
Association analyses identify 31 new risk loci for colorectal cancer susceptibility.
31089142
2019
rs12427600
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Malignant neoplasm of large intestine
C
0.700
GeneticVariation
GWASCAT
Association analyses identify 31 new risk loci for colorectal cancer susceptibility.
31089142
2019
rs12427600
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Colorectal Carcinoma
C
0.700
GeneticVariation
GWASCAT
Association analyses identify 31 new risk loci for colorectal cancer susceptibility.
31089142
2019
rs12427600
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
C
0.700
GeneticVariation
GWASCAT
Association analyses identify 31 new risk loci for colorectal cancer susceptibility.
31089142
2019
rs7333607
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Malignant neoplasm of large intestine
G
0.700
GeneticVariation
GWASCAT
Discovery of common and rare genetic risk variants for colorectal cancer.
30510241
2019
rs7333607
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
G
0.700
GeneticVariation
GWASCAT
Discovery of common and rare genetic risk variants for colorectal cancer.
30510241
2019
rs7333607
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
G
0.700
GeneticVariation
GWASCAT
Discovery of common and rare genetic risk variants for colorectal cancer.
30510241
2019
rs7333607
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Adenocarcinoma of large intestine
G
0.700
GeneticVariation
GWASCAT
Discovery of common and rare genetic risk variants for colorectal cancer.
30510241
2019
rs7333607
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Colorectal Carcinoma
G
0.700
GeneticVariation
GWASCAT
Discovery of common and rare genetic risk variants for colorectal cancer.
30510241
2019
rs7333607
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Malignant tumor of colon
G
0.700
GeneticVariation
GWASCAT
Discovery of common and rare genetic risk variants for colorectal cancer.
30510241
2019
rs7333607
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
G
0.700
GeneticVariation
GWASCAT
Discovery of common and rare genetic risk variants for colorectal cancer.
30510241
2019
rs7333607
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Adenoma of large intestine
G
0.700
GeneticVariation
GWASCAT
Discovery of common and rare genetic risk variants for colorectal cancer.
30510241
2019
rs7333607
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
G
0.700
GeneticVariation
GWASCAT
Discovery of common and rare genetic risk variants for colorectal cancer.
30510241
2019
rs7333607
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Colorectal Neoplasms
G
0.700
GeneticVariation
GWASCAT
Discovery of common and rare genetic risk variants for colorectal cancer.
30510241
2019
rs9576132
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Body Height
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs121918359
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Essential Hypertension
0.010
GeneticVariation
BEFREE
The CG haplotype of the rs6435156 and rs1048829 loci of the <i>BMPR2</i> gene, the CC haplotype of the <i>ACVRL1</i> gene rs121909287 and rs121909284 loci, and the CC haplotype of the rs397514716 and rs121918359 loci of the <i>SMAD9</i> gene were factors that protect against EH , whereas the TT haplotype of the rs6435156 and rs1048829 loci in the <i>BMPR2</i> gene was a risk factor for EH.
30617053
2019
rs371433324
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Hypospadias
0.010
GeneticVariation
BEFREE
The unique features of SRD5A2 defects were p.R246Q (most prevalent) and p.G196S could be mutational hotspots, dual gene defects (p.A596T in AR and p.G196S in SRD5A2) in a patient with hypospadias and novel 8 nucleotide deletion (exon 1) found in a patient with perineal hypospadias.
30550360
2019
rs371433324
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Hypospadias, perineal
0.010
GeneticVariation
BEFREE
The unique features of SRD5A2 defects were p.R246Q (most prevalent) and p.G196S could be mutational hotspots, dual gene defects (p.A596T in AR and p.G196S in SRD5A2) in a patient with hypospadias and novel 8 nucleotide deletion (exon 1) found in a patient with perineal hypospadias .
30550360
2019
rs371433324
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Penile hypospadias
0.010
GeneticVariation
BEFREE
The unique features of SRD5A2 defects were p.R246Q (most prevalent) and p.G196S could be mutational hotspots, dual gene defects (p.A596T in AR and p.G196S in SRD5A2) in a patient with hypospadias and novel 8 nucleotide deletion (exon 1) found in a patient with perineal hypospadias.
30550360
2019
rs397514716
×
Entrez Id:
4093
Gene Symbol:
SMAD9
SMAD9
Essential Hypertension
0.010
GeneticVariation
BEFREE
The risk of EH increased in the <i>SMAD9</i> gene rs397514716 locus dominant model (adjusted OR = 1.370, 95% CI: 1.183 -1.559, <i>P</i><0.001) and recessive mo del (adjusted OR = 1.803, 95 % CI: 1.470-1.983, <i>P</i><0.001).
30617053
2019