Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1378942
rs1378942
CSK
16 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 4 2011 2019
dbSNP: rs16849225
rs16849225
5 2 164050310 intron variant C/T snv 0.19 0.700 1.000 4 2011 2018
dbSNP: rs16998073
rs16998073
10 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 0.700 1.000 4 2017 2019
dbSNP: rs1801253
rs1801253
34 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.700 1.000 4 2016 2019
dbSNP: rs2306363
rs2306363
7 11 65638129 5 prime UTR variant G/T snv 0.15 0.700 1.000 4 2017 2019
dbSNP: rs2643826
rs2643826
6 3 27521497 upstream gene variant C/T snv 0.56 0.700 1.000 4 2017 2019
dbSNP: rs2898290
rs2898290
2 8 11576400 non coding transcript exon variant T/C snv 0.49 0.700 1.000 4 2016 2018
dbSNP: rs419076
rs419076
6 3 169383098 intron variant T/A;C snv 0.700 1.000 4 2011 2018
dbSNP: rs569550
rs569550
6 0.925 0.080 11 1865838 intron variant T/G snv 0.35 0.700 1.000 4 2018 2019
dbSNP: rs6015450
rs6015450
7 20 59176062 intron variant A/G snv 0.14 0.700 1.000 4 2011 2018
dbSNP: rs8904
rs8904
4 0.925 0.120 14 35402011 3 prime UTR variant G/A;C;T snv 0.39; 4.0E-06 0.700 1.000 4 2017 2019
dbSNP: rs932764
rs932764
6 10 94136183 intron variant A/G snv 0.38 0.700 1.000 4 2011 2017
dbSNP: rs1004467
rs1004467
13 0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 0.700 1.000 3 2009 2018
dbSNP: rs10260816
rs10260816
2 7 45970501 intron variant C/A;G;T snv 0.700 1.000 3 2017 2019
dbSNP: rs10437954
rs10437954
1 12 57610139 upstream gene variant G/A;C snv 0.700 1.000 3 2018 2019
dbSNP: rs10857147
rs10857147
9 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 0.700 1.000 3 2018 2019
dbSNP: rs10948071
rs10948071
4 6 43312975 intron variant C/T snv 0.46 0.700 1.000 3 2017 2018
dbSNP: rs11066280
rs11066280
27 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 3 2011 2015
dbSNP: rs11099098
rs11099098
8 0.925 0.120 4 80248758 intergenic variant G/C;T snv 0.700 1.000 3 2014 2019
dbSNP: rs11191580
rs11191580
13 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 0.700 1.000 3 2017 2019
dbSNP: rs11222084
rs11222084
3 11 130403335 non coding transcript exon variant A/T snv 0.30 0.700 1.000 3 2017 2019
dbSNP: rs1126930
rs1126930
5 12 49005349 missense variant G/C snv 2.1E-02 2.1E-02 0.700 1.000 3 2016 2019
dbSNP: rs1173766
rs1173766
5 5 32804422 intergenic variant T/C snv 0.57 0.700 1.000 3 2011 2018
dbSNP: rs139491786
rs139491786
4 16 2036420 missense variant C/T snv 3.4E-03 3.5E-03 0.700 1.000 3 2017 2019
dbSNP: rs1446468
rs1446468
4 2 164106976 intron variant T/C snv 0.40 0.700 1.000 3 2017 2018