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: rs16998073
rs16998073
10 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 0.700 1.000 2 2011 2011
dbSNP: rs10444602
rs10444602
1 12 131708291 upstream gene variant T/G snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs11099098
rs11099098
8 0.925 0.120 4 80248758 intergenic variant G/C;T snv 0.700 1.000 1 2014 2014
dbSNP: rs11659639
rs11659639
1 18 60500379 intron variant T/G snv 1.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs1173766
rs1173766
5 5 32804422 intergenic variant T/C snv 0.57 0.700 1.000 1 2011 2011
dbSNP: rs1173771
rs1173771
9 5 32814922 regulatory region variant A/G snv 0.65 0.700 1.000 1 2011 2011
dbSNP: rs11816631
rs11816631
1 10 97802815 intergenic variant A/G snv 8.8E-02 0.700 1.000 1 2014 2014
dbSNP: rs12067906
rs12067906
1 1 192462868 intron variant T/C snv 0.12 0.800 1.000 1 2012 2012
dbSNP: rs12098903
rs12098903
1 11 55899037 downstream gene variant A/T snv 5.7E-02 0.700 1.000 1 2011 2011
dbSNP: rs12098904
rs12098904
1 11 55899077 downstream gene variant A/T snv 5.7E-02 0.700 1.000 1 2011 2011
dbSNP: rs12098941
rs12098941
1 11 55898967 downstream gene variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs12627514
rs12627514
3 1.000 0.040 21 43339560 intergenic variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs13002573
rs13002573
3 2 164058698 intron variant A/G snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs13040716
rs13040716
2 1.000 0.040 20 32182402 downstream gene variant A/G snv 1.0E-01 0.700 1.000 1 2019 2019
dbSNP: rs13082711
rs13082711
5 3 27496418 intergenic variant T/C snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs13149993
rs13149993
6 4 80237391 regulatory region variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs13209747
rs13209747
5 6 126794309 intron variant C/G;T snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs1327235
rs1327235
7 20 10988382 intron variant A/G snv 0.46 0.700 1.000 1 2011 2011
dbSNP: rs1384089
rs1384089
1 11 56081540 upstream gene variant G/C snv 6.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs1446468
rs1446468
4 2 164106976 intron variant T/C snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs1458038
rs1458038
10 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs1492840
rs1492840
1 4 45764988 intergenic variant A/C;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs16833934
rs16833934
3 3 164019462 intergenic variant A/G snv 0.34 0.700 1.000 1 2014 2014
dbSNP: rs16849225
rs16849225
5 2 164050310 intron variant C/T snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs16877320
rs16877320
2 6 15922795 TF binding site variant T/A;C snv 0.700 1.000 1 2011 2011