Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0009402
Disease:
Colorectal Carcinoma 		T 0.800 GeneticVariation GWASDB Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. 23263487 2013
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0009402
Disease:
Colorectal Carcinoma 		T 0.800 GeneticVariation GWASCAT Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. 23263487 2013
dbSNP: rs11592166
rs11592166
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0871470
Disease:
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs11197813
rs11197813
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653 2018
dbSNP: rs12259842
rs12259842
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0025209
Disease:
Melanosis 		T 0.700 GeneticVariation GWASCAT Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations. 29895819 2018
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. 23263487 2013
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0346629
Disease:
Malignant neoplasm of large intestine 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. 23263487 2013
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0009404
Disease:
Colorectal Neoplasms 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. 23263487 2013
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0007102
Disease:
Malignant tumor of colon 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. 23263487 2013
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. 23263487 2013
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. 23263487 2013
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C1319315
Disease:
Adenocarcinoma of large intestine 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. 23263487 2013
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. 23263487 2013
dbSNP: rs17095224
rs17095224
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0595989
Disease:
Carcinoma of larynx 		0.010 GeneticVariation BEFREE Univariate cox regression analysis indicated that four SNPs were associated (p < 0.05) with LC OS in the codominant genetic model compared to patients with the homozygous wild-type genotype: rs10088262 G/A (HR = 1.57), rs1665650 A/G (HR = 0.65); rs3802842 C/C (HR = 2.18), and rs59336 T/A and T/T (HR = 0.61 and 2.61, respectively). 28052013 2017
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0699791
Disease:
Stomach Carcinoma 		0.010 GeneticVariation BEFREE The genotype "A/G" of rs1665650 in HSPA12A gene was associated with a decreased risk of gastric cancer in overdominant model analysis (OR = 0.77; 95% CI = 0.60-0.99; p = 0.038). 26302849 2015
dbSNP: rs1665650
rs1665650
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.010 GeneticVariation BEFREE The genotype "A/G" of rs1665650 in HSPA12A gene was associated with a decreased risk of gastric cancer in overdominant model analysis (OR = 0.77; 95% CI = 0.60-0.99; p = 0.038). 26302849 2015
dbSNP: rs740363
rs740363
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0007222
Disease:
Cardiovascular Diseases 		0.010 GeneticVariation BEFREE Six associations yielded p < 10(-5).The lowest p-values for each CVD trait were as follows: major CVD, rs499818, p = 6.6 x 10(-6); major CHD, rs2549513, p = 9.7 x 10(-6); AF, rs958546, p = 4.8 x 10(-6); HF: rs740363, p = 8.8 x 10(-6). 17903304 2007
dbSNP: rs740363
rs740363
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0004238
Disease:
Atrial Fibrillation 		0.010 GeneticVariation BEFREE Six associations yielded p < 10(-5).The lowest p-values for each CVD trait were as follows: major CVD, rs499818, p = 6.6 x 10(-6); major CHD, rs2549513, p = 9.7 x 10(-6); AF, rs958546, p = 4.8 x 10(-6); HF: rs740363, p = 8.8 x 10(-6). 17903304 2007
dbSNP: rs740363
rs740363
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0018801
Disease:
Heart failure 		0.010 GeneticVariation BEFREE Six associations yielded p < 10(-5).The lowest p-values for each CVD trait were as follows: major CVD, rs499818, p = 6.6 x 10(-6); major CHD, rs2549513, p = 9.7 x 10(-6); AF, rs958546, p = 4.8 x 10(-6); HF: rs740363, p = 8.8 x 10(-6). 17903304 2007
dbSNP: rs740363
rs740363
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0018802
Disease:
Congestive heart failure 		0.010 GeneticVariation BEFREE Six associations yielded p < 10(-5).The lowest p-values for each CVD trait were as follows: major CVD, rs499818, p = 6.6 x 10(-6); major CHD, rs2549513, p = 9.7 x 10(-6); AF, rs958546, p = 4.8 x 10(-6); HF: rs740363, p = 8.8 x 10(-6). 17903304 2007
dbSNP: rs740363
rs740363
Entrez Id: 259217
Gene Symbol: HSPA12A
HSPA12A
CUI: C0010068
Disease:
Coronary heart disease 		0.010 GeneticVariation BEFREE Six associations yielded p < 10(-5).The lowest p-values for each CVD trait were as follows: major CVD, rs499818, p = 6.6 x 10(-6); major CHD, rs2549513, p = 9.7 x 10(-6); AF, rs958546, p = 4.8 x 10(-6); HF: rs740363, p = 8.8 x 10(-6). 17903304 2007