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: rs1057519824
rs1057519824
0.807 0.120 7 116783374 missense variant T/G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
Neoplasms 0.700 1.000 1 2002 2002
dbSNP: rs1057520030
rs1057520030
7 116777427 missense variant A/G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
Neoplasms 0.700 1.000 1 2002 2002
dbSNP: rs121913245
rs121913245
0.925 0.120 7 116783420 missense variant T/C snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
Neoplasms 0.700 1.000 1 1998 1998
dbSNP: rs121913246
rs121913246
0.827 0.200 7 116783360 missense variant A/G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
Neoplasms 0.700 1.000 1 1998 1998
dbSNP: rs121913671
rs121913671
0.882 0.160 7 116783353 missense variant G/A;C snv
CUI: C0007097
Disease: Carcinoma
Carcinoma
Neoplasms 0.700 1.000 1 1998 1998
dbSNP: rs56391007
rs56391007
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03
CUI: C0007097
Disease: Carcinoma
Carcinoma
Neoplasms 0.700 1.000 1 1975 1975
dbSNP: rs786202724
rs786202724
0.925 0.120 7 116777403 missense variant G/A snv 7.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
Neoplasms 0.700 1.000 1 1999 1999