Source: UNIPROT

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: rs63750664
rs63750664
MSH6
0.882 0.200 2 47783292 missense variant C/A;T snv 4.1E-06; 9.4E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 12 1999 2012
dbSNP: rs63750664
rs63750664
MSH6
0.882 0.200 2 47783292 missense variant C/A;T snv 4.1E-06; 9.4E-05
CUI: C1833477
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5 		0.700 1.000 9 1997 2012
dbSNP: rs63750664
rs63750664
MSH6
0.882 0.200 2 47783292 missense variant C/A;T snv 4.1E-06; 9.4E-05
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.700 1.000 2 2000 2004