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: rs61753793
rs61753793
MSH6 ; FBXO11
0.851 0.120 2 47799002 missense variant T/C snv 3.6E-05 5.6E-05
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.710 1.000 0 2000 2000
dbSNP: rs61753793
rs61753793
MSH6 ; FBXO11
0.851 0.120 2 47799002 missense variant T/C snv 3.6E-05 5.6E-05
CUI: C0023418
Disease: leukemia
leukemia 		0.700 0
dbSNP: rs61753793
rs61753793
MSH6 ; FBXO11
0.851 0.120 2 47799002 missense variant T/C snv 3.6E-05 5.6E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 0