LAMA5, laminin subunit alpha 5, 3911

N. diseases: 56; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE The association of LAMA5 rs4925386 alleles with both inter-individual differences in height and in longevity suggests that laminins may be among the factors linking stature and cancer susceptibility. 26968355 2016
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE The association of LAMA5 rs4925386 alleles with both inter-individual differences in height and in longevity suggests that laminins may be among the factors linking stature and cancer susceptibility. 26968355 2016
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C4722085
Disease:
Malignant neoplasm of colon and/or rectum
0.010 GeneticVariation BEFREE Notably, two independent meta-analyses of genome-wide association studies found the C-allele of LAMA5 rs4925386-C/T correlated with the risk of colorectal cancer. 26968355 2016
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C0001430
Disease:
Adenoma
0.010 GeneticVariation BEFREE Ten other CRC-associated SNPs (rs6691170, rs6687758, rs16892766, rs7136702, rs11169552, rs4779584, rs9929218, rs10411210, rs4813802, and rs4925386) were not associated significantly with adenoma risk. 22999960 2013
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C0009373
Disease:
Colonic Diseases
0.010 GeneticVariation BEFREE Several loci showed statistically significant associations with specific phenotypes notably rs6691170 and rs3802842 associated with microsatellite stable rectal disease; rs4779584, rs961253 and rs4813802 associated with microsatellite stable colonic disease and rs4444235 and rs4925386 with microsatellite instability colonic disease. 22045029 2012
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C0009402
Disease:
Colorectal Carcinoma
C 0.830 GeneticVariation GWASDB We identified associations at four new CRC risk loci: 1q41 (rs6691170, odds ratio (OR) = 1.06, P = 9.55 × 10⁻¹⁰ and rs6687758, OR = 1.09, P = 2.27 × 10⁻⁹, 3q26.2 (rs10936599, OR = 0.93, P = 3.39 × 10⁻⁸), 12q13.13 (rs11169552, OR = 0.92, P = 1.89 × 10⁻¹⁰ and rs7136702, OR = 1.06, P = 4.02 × 10⁻⁸) and 20q13.33 (rs4925386, OR = 0.93, P = 1.89 × 10⁻¹⁰). 20972440 2010
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C0009402
Disease:
Colorectal Carcinoma
C 0.830 GeneticVariation GWASCAT We identified associations at four new CRC risk loci: 1q41 (rs6691170, odds ratio (OR) = 1.06, P = 9.55 × 10⁻¹⁰ and rs6687758, OR = 1.09, P = 2.27 × 10⁻⁹, 3q26.2 (rs10936599, OR = 0.93, P = 3.39 × 10⁻⁸), 12q13.13 (rs11169552, OR = 0.92, P = 1.89 × 10⁻¹⁰ and rs7136702, OR = 1.06, P = 4.02 × 10⁻⁸) and 20q13.33 (rs4925386, OR = 0.93, P = 1.89 × 10⁻¹⁰). 20972440 2010
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C0009402
Disease:
Colorectal Carcinoma
0.830 GeneticVariation BEFREE We identified associations at four new CRC risk loci: 1q41 (rs6691170, odds ratio (OR) = 1.06, P = 9.55 × 10⁻¹⁰ and rs6687758, OR = 1.09, P = 2.27 × 10⁻⁹, 3q26.2 (rs10936599, OR = 0.93, P = 3.39 × 10⁻⁸), 12q13.13 (rs11169552, OR = 0.92, P = 1.89 × 10⁻¹⁰ and rs7136702, OR = 1.06, P = 4.02 × 10⁻⁸) and 20q13.33 (rs4925386, OR = 0.93, P = 1.89 × 10⁻¹⁰). 20972440 2010
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
C 0.700 GeneticVariation GWASCAT Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. 20972440 2010
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
C 0.700 GeneticVariation GWASCAT Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. 20972440 2010
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C0346629
Disease:
Malignant neoplasm of large intestine
C 0.700 GeneticVariation GWASCAT Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. 20972440 2010
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C0007102
Disease:
Malignant tumor of colon
C 0.700 GeneticVariation GWASCAT Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. 20972440 2010
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
C 0.700 GeneticVariation GWASCAT Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. 20972440 2010
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
C 0.700 GeneticVariation GWASCAT Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. 20972440 2010
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C1319315
Disease:
Adenocarcinoma of large intestine
C 0.700 GeneticVariation GWASCAT Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. 20972440 2010
dbSNP: rs4925386
rs4925386
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C0009404
Disease:
Colorectal Neoplasms
C 0.700 GeneticVariation GWASCAT Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. 20972440 2010
dbSNP: rs370433088
rs370433088
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C0349588
Disease:
Short stature
T 0.700 GeneticVariation CLINVAR
dbSNP: rs756101090
rs756101090
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C1305904
Disease:
Familial hematuria
A 0.700 CausalMutation CLINVAR
dbSNP: rs766464011
rs766464011
Entrez Id: 3911;100616340
Gene Symbol: LAMA5;MIR4758
LAMA5;MIR4758
CUI: C0349588
Disease:
Short stature
T 0.700 GeneticVariation CLINVAR
dbSNP: rs773956500
rs773956500
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C0349588
Disease:
Short stature
C 0.700 GeneticVariation CLINVAR