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: rs3769839
rs3769839
0.925 0.080 2 230211910 intron variant T/C snv 0.12
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.700 1.000 1 2018 2018
dbSNP: rs7731017
rs7731017
0.925 0.080 5 150732056 intron variant T/C snv 8.3E-03
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.700 1.000 1 2018 2018
dbSNP: rs12979860
rs12979860
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.020 1.000 2 2013 2016
dbSNP: rs1003723
rs1003723
0.925 0.080 19 11113505 non coding transcript exon variant C/A;T snv 4.0E-06; 0.40
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2008 2008
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2013 2013
dbSNP: rs104886003
rs104886003
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2019 2019
dbSNP: rs1126579
rs1126579
0.776 0.200 2 218136011 3 prime UTR variant T/C snv 0.62
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2008 2008
dbSNP: rs1126580
rs1126580
0.882 0.120 2 218136243 3 prime UTR variant G/A;T snv
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2008 2008
dbSNP: rs113488022
rs113488022
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2019 2019
dbSNP: rs11635252
rs11635252
0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2018 2018
dbSNP: rs11887534
rs11887534
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2011 2011
dbSNP: rs1194919682
rs1194919682
0.925 0.040 2 136115158 missense variant A/G snv
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2012 2012
dbSNP: rs1217691063
rs1217691063
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2007 2007
dbSNP: rs121913377
rs121913377
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2019 2019
dbSNP: rs17851045
rs17851045
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2019 2019
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2013 2013
dbSNP: rs2072671
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2019 2019
dbSNP: rs2076310
rs2076310
0.925 0.080 6 33198257 intron variant A/G snv 0.27 0.28
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2008 2008
dbSNP: rs2106261
rs2106261
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2018 2018
dbSNP: rs2230054
rs2230054
0.925 0.080 2 218135587 synonymous variant C/T snv 0.48 0.54
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2008 2008
dbSNP: rs2266788
rs2266788
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2018 2018
dbSNP: rs2287622
rs2287622
0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2011 2011
dbSNP: rs2289278
rs2289278
0.827 0.200 5 111073450 5 prime UTR variant C/G snv 8.7E-02
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2016 2016
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2013 2013
dbSNP: rs25489
rs25489
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2013 2013