MSH5, mutS homolog 5, 4439

N. diseases: 51; N. variants: 23
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1144709
rs1144709
Entrez Id: 4439;100532732;105375020
Gene Symbol: MSH5;MSH5-SAPCD1;LOC105375020
MSH5;MSH5-SAPCD1;LOC105375020
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: rs1144709
rs1144709
Entrez Id: 4439;100532732;105375020
Gene Symbol: MSH5;MSH5-SAPCD1;LOC105375020
MSH5;MSH5-SAPCD1;LOC105375020
CUI: C0596887
Disease:
mathematical ability
C 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