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: rs10025419
rs10025419
1 4 100647799 intron variant G/A snv 0.87 0.700 1.000 1 2015 2015
dbSNP: rs10041590
rs10041590
2 5 24064827 intron variant T/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs10054178
rs10054178
2 5 24059742 intron variant A/G snv 7.5E-02 0.700 1.000 1 2015 2015
dbSNP: rs10056373
rs10056373
2 5 24069684 intron variant C/T snv 7.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs10119043
rs10119043
2 9 135122706 downstream gene variant C/T snv 0.11 0.700 1.000 1 2015 2015
dbSNP: rs10178992
rs10178992
4 2 233749231 intron variant T/A snv 0.37 0.700 1.000 1 2015 2015
dbSNP: rs10179091
rs10179091
4 2 233749337 intron variant T/C snv 0.49 0.700 1.000 1 2015 2015
dbSNP: rs10827209
rs10827209
2 10 33198261 intron variant A/C snv 0.23 0.700 1.000 1 2015 2015
dbSNP: rs10892961
rs10892961
2 11 123093392 intron variant A/C;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10929301
rs10929301
4 2 233755003 splice region variant C/G;T snv 0.48 0.700 1.000 1 2015 2015
dbSNP: rs10929302
rs10929302
4 2 233757136 intron variant G/A snv 0.30 0.700 1.000 1 2015 2015
dbSNP: rs11011237
rs11011237
2 10 37531016 intron variant G/A snv 9.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs11087114
rs11087114
1 20 14931037 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs11218976
rs11218976
2 11 123090950 intron variant A/G snv 0.41 0.700 1.000 1 2015 2015
dbSNP: rs11228672
rs11228672
2 11 56597931 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs113051092
rs113051092
2 5 24060490 intron variant A/T snv 7.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs113162402
rs113162402
1 17 58522103 splice acceptor variant T/A snv 0.700 1.000 1 2015 2015
dbSNP: rs11673726
rs11673726
4 2 233755414 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs11695484
rs11695484
3 2 233745803 intron variant A/G snv 0.30 0.700 1.000 1 2015 2015
dbSNP: rs116965780
rs116965780
2 18 43300829 intergenic variant C/T snv 7.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs11888459
rs11888459
4 2 233747994 non coding transcript exon variant T/C snv 0.37 0.700 1.000 1 2015 2015
dbSNP: rs11914494
rs11914494
2 3 119121264 intron variant G/A snv 1.8E-02 0.700 1.000 1 2015 2015
dbSNP: rs11926663
rs11926663
2 3 119125638 intron variant A/G snv 1.8E-02 0.700 1.000 1 2015 2015
dbSNP: rs12587266
rs12587266
1 14 92580298 intron variant A/G snv 0.63 0.700 1.000 1 2015 2015
dbSNP: rs139231591
rs139231591
1 3 48342403 regulatory region variant C/T snv 1.2E-02 0.700 1.000 1 2015 2015