Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs864622258
rs864622258
MLH1
0.925 0.160 3 37050610 missense variant T/G snv 1.4E-05
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
Hereditary Nonpolyposis Colorectal Cancer 		0.010 1.000 1 2006 2006
dbSNP: rs864622258
rs864622258
MLH1
0.925 0.160 3 37050610 missense variant T/G snv 1.4E-05
CUI: C4552100
Disease: Lynch Syndrome
Lynch Syndrome 		0.010 1.000 1 2006 2006