Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13255193
rs13255193
Entrez Id: 83648
Gene Symbol: FAM167A
FAM167A
CUI: C0871470
Disease:
Systolic Pressure 		T 0.700 GeneticVariation GWASCAT Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. 29912962 2018
dbSNP: rs13255193
rs13255193
Entrez Id: 83648
Gene Symbol: FAM167A
FAM167A
CUI: C1306620
Disease:
Systolic blood pressure measurement 		T 0.700 GeneticVariation GWASCAT Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. 29912962 2018
dbSNP: rs4841531
rs4841531
Entrez Id: 83648;83656
Gene Symbol: FAM167A;FAM167A-AS1
FAM167A;FAM167A-AS1
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. 29455858 2018
dbSNP: rs61649748
rs61649748
Entrez Id: 83648
Gene Symbol: FAM167A
FAM167A
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs12156238
rs12156238
Entrez Id: 83648;83656
Gene Symbol: FAM167A;FAM167A-AS1
FAM167A;FAM167A-AS1
CUI: C0235280
Disease:
Ototoxicity 		C 0.700 GeneticVariation GWASCAT Variants in WFS1 and Other Mendelian Deafness Genes Are Associated with Cisplatin-Associated Ototoxicity. 28039263 2017
dbSNP: rs2409764
rs2409764
Entrez Id: 83648;83656
Gene Symbol: FAM167A;FAM167A-AS1
FAM167A;FAM167A-AS1
CUI: C0014859
Disease:
Esophageal Neoplasms 		0.700 GeneticVariation GWASDB Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions. 22960999 2012
dbSNP: rs886037620
rs886037620
Entrez Id: 83648
Gene Symbol: FAM167A
FAM167A
CUI: C3150618
Disease:
Maturity-onset diabetes of the young, type 11 		A 0.700 CausalMutation CLINVAR
dbSNP: rs2618431
rs2618431
Entrez Id: 83648
Gene Symbol: FAM167A
FAM167A
CUI: C3840565
Disease:
Autoimmune thyroid disease (AITD) 		0.010 GeneticVariation BEFREE Similarly, compared with that in female controls, allele G of rs2618431 was increased in the female AITD patients. 30351170 2018
dbSNP: rs2618431
rs2618431
Entrez Id: 83648
Gene Symbol: FAM167A
FAM167A
CUI: C0018213
Disease:
Graves Disease 		0.010 GeneticVariation BEFREE Likewise, the frequency of allele G in rs2618431 obviously declined in the female G</span>D patients. 30351170 2018