MSH2, mutS homolog 2, 4436

N. diseases: 490; N. variants: 777
Disease: Glioma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63751110
rs63751110
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0017638
Disease:
Glioma 		0.700 GeneticVariation UNIPROT