MSH6, mutS homolog 6, 2956

N. diseases: 296; N. variants: 642
Disease: Pancreatic carcinoma, familial ×
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: rs1187393388
rs1187393388 		1.000 0.120 2 47800567 missense variant C/G;T snv 4.0E-06
CUI: C2931038
Disease: Pancreatic carcinoma, familial
Pancreatic carcinoma, familial 		Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs587779930
rs587779930 		1.000 0.120 2 47801083 missense variant C/G;T snv 4.0E-06; 1.6E-05
CUI: C2931038
Disease: Pancreatic carcinoma, familial
Pancreatic carcinoma, familial 		Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs63751127
rs63751127 		0.882 0.200 2 47800177 stop gained C/A;T snv 4.0E-06; 4.0E-06
CUI: C2931038
Disease: Pancreatic carcinoma, familial
Pancreatic carcinoma, familial 		Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.010 1.000 1 2020 2020