MSH2, mutS homolog 2, 4436

N. diseases: 490; N. variants: 777
Disease: Glioma ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs63751110
rs63751110 		0.925 0.160 2 47410322 missense variant T/C;G snv
CUI: C0017638
Disease: Glioma
Glioma 		Neoplasms 0.700 0