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: rs587778937
rs587778937
0.882 0.160 3 37040291 missense variant T/C;G snv
Hereditary Nonpolyposis Colorectal Cancer
0.710 1.000 1 2013 2013
dbSNP: rs587778937
rs587778937
0.882 0.160 3 37040291 missense variant T/C;G snv
CUI: C4523846
Disease: MSI-high
MSI-high
0.010 1.000 1 2013 2013
dbSNP: rs587778937
rs587778937
0.882 0.160 3 37040291 missense variant T/C;G snv
CUI: C4552100
Disease: Lynch Syndrome
Lynch Syndrome
0.010 1.000 1 2013 2013
dbSNP: rs587778937
rs587778937
0.882 0.160 3 37040291 missense variant T/C;G snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2013 2013