SORBS2, sorbin and SH3 domain containing 2, 8470

N. diseases: 25; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2310357
rs2310357
Entrez Id: 8470
Gene Symbol: SORBS2
SORBS2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs2310357
rs2310357
Entrez Id: 8470
Gene Symbol: SORBS2
SORBS2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11728712
rs11728712
Entrez Id: 8470
Gene Symbol: SORBS2
SORBS2
CUI: C0596887
Disease:
mathematical ability
G 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: rs6838265
rs6838265
Entrez Id: 8470
Gene Symbol: SORBS2
SORBS2
CUI: C0596887
Disease:
mathematical ability
A 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: rs6838265
rs6838265
Entrez Id: 8470
Gene Symbol: SORBS2
SORBS2
CUI: C0596887
Disease:
mathematical ability
G 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: rs7654779
rs7654779
Entrez Id: 8470
Gene Symbol: SORBS2
SORBS2
CUI: C0596887
Disease:
mathematical ability
A 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: rs4862562
rs4862562
Entrez Id: 8470
Gene Symbol: SORBS2
SORBS2
CUI: C3897558
Disease:
Soluble Interleukin 6 Receptor Measurement
C 0.700 GeneticVariation GWASCAT VPS13D Gene Variant Is Associated with Altered IL-6 Production and Mortality in Septic Shock. 25896417 2015
dbSNP: rs1566347
rs1566347
Entrez Id: 8470
Gene Symbol: SORBS2
SORBS2
CUI: C0029408
Disease:
Degenerative polyarthritis
0.700 GeneticVariation GWASDB Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study. 22763110 2012
dbSNP: rs1274124656
rs1274124656
Entrez Id: 8470
Gene Symbol: SORBS2
SORBS2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE We previously found a significant association between the T228A polymorphism and insulin resistance, obesity, and type 2 diabetes. 26962801 2016
dbSNP: rs1437921067
rs1437921067
Entrez Id: 8470
Gene Symbol: SORBS2
SORBS2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE We previously found a significant association between the T228A polymorphism and insulin resistance, obesity, and type 2 diabetes. 26962801 2016
dbSNP: rs139155954
rs139155954
Entrez Id: 8470
Gene Symbol: SORBS2
SORBS2
CUI: C0276496
Disease:
Familial Alzheimer Disease (FAD)
0.010 GeneticVariation BEFREE Genetic Modifiers of Age at Onset in Carriers of the G206A Mutation in PSEN1 With Familial Alzheimer Disease Among Caribbean Hispanics. 26214276 2015
dbSNP: rs773029808
rs773029808
Entrez Id: 8470
Gene Symbol: SORBS2
SORBS2
CUI: C0276496
Disease:
Familial Alzheimer Disease (FAD)
0.010 GeneticVariation BEFREE Genetic Modifiers of Age at Onset in Carriers of the G206A Mutation in PSEN1 With Familial Alzheimer Disease Among Caribbean Hispanics. 26214276 2015