Source: ALL

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: rs26279
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.020 1.000 2 2009 2015
dbSNP: rs26279
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.020 1.000 2 2009 2015
dbSNP: rs26279
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 1.000 2 2012 2015
dbSNP: rs26279
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 1.000 2 2012 2015
dbSNP: rs26279
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs26279
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70
CUI: C0004509
Disease: Azoospermia
Azoospermia 		0.010 1.000 1 2019 2019
dbSNP: rs26279
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs26279
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.010 1.000 1 2015 2015
dbSNP: rs26279
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2015 2015