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: rs10748798
rs10748798
1 10 100794914 intron variant C/T snv 0.91 0.700 1.000 1 2019 2019
dbSNP: rs10769254
rs10769254
4 11 47340914 intron variant G/C snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs10786156
rs10786156
2 10 94254865 intron variant C/G snv 0.44 0.47 0.700 1.000 1 2019 2019
dbSNP: rs10816914
rs10816914
1 9 109998608 intron variant G/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs10821967
rs10821967
1 10 62182180 downstream gene variant A/G snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs10824134
rs10824134
ADK
1 10 74261866 intron variant T/C snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs10832571
rs10832571
1 11 16239678 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs10849891
rs10849891
1 12 121473799 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10850407
rs10850407
1 12 114940232 intergenic variant T/G snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs10872673
rs10872673
1 6 151534458 intron variant G/T snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10882397
rs10882397
2 10 94132902 intron variant C/A snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs10942863
rs10942863
1 5 78550731 intron variant C/G;T snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs11017236
rs11017236
1 10 130401217 intron variant T/A snv 0.28 0.700 1.000 1 2008 2008
dbSNP: rs11048457
rs11048457
1 12 26310241 intron variant G/A snv 0.62 0.700 1.000 1 2019 2019
dbSNP: rs11072508
rs11072508
2 1.000 0.080 15 74770056 regulatory region variant C/T snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs11111839
rs11111839
1 12 103916945 intron variant C/A snv 7.9E-02 0.700 1.000 1 2008 2008
dbSNP: rs11130381
rs11130381
1 3 53815978 3 prime UTR variant C/T snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs11191580
rs11191580
13 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs11229555
rs11229555
7 0.827 0.120 11 58641214 intron variant G/T snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs11231711
rs11231711
1 11 64161743 intron variant G/A snv 8.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs112684153
rs112684153
1 13 41275595 intergenic variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs113230003
rs113230003
2 19 18350146 intron variant G/A snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs113602013
rs113602013
1 18 60252477 intergenic variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs113898337
rs113898337
1 2 20567381 intron variant C/G snv 4.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs1149643
rs1149643
1 1 56163763 intron variant A/T snv 0.49 0.700 1.000 1 2019 2019