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: rs501120
rs501120
10 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 0.020 1.000 2 2012 2019
dbSNP: rs10042590
rs10042590
1 5 88477501 intron variant G/A snv 5.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs10059884
rs10059884
5 5 32832368 regulatory region variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1030431
rs1030431
3 8 58399138 intergenic variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10759931
rs10759931
9 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 0.010 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: rs10938397
rs10938397
19 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 0.010 1.000 1 2010 2010
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: rs11084753
rs11084753
6 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 0.010 1.000 1 2010 2010
dbSNP: rs11206510
rs11206510
16 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 0.010 1.000 1 2017 2017
dbSNP: rs113602013
rs113602013
1 18 60252477 intergenic variant G/A;C snv 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
dbSNP: rs1154988
rs1154988
7 3 136206349 upstream gene variant T/A snv 0.76 0.700 1.000 1 2019 2019
dbSNP: rs11605518
rs11605518
1 11 13248667 intergenic variant A/G snv 0.72 0.700 1.000 1 2019 2019
dbSNP: rs11688682
rs11688682
3 1.000 0.080 2 120590036 intergenic variant G/C snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs11826048
rs11826048
1 11 103527569 intergenic variant C/T snv 9.6E-02 0.700 1.000 1 2008 2008
dbSNP: rs12324159
rs12324159
1 15 41170270 regulatory region variant G/A snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs12358504
rs12358504
1 10 121240352 intergenic variant A/G snv 0.18 0.700 1.000 1 2019 2019
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: rs13021222
rs13021222
1 2 164191395 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs13125101
rs13125101
6 4 80253438 TF binding site variant G/A snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs13210511
rs13210511
2 6 126834566 intron variant C/T snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs13265769
rs13265769
1 8 81912028 intron variant T/C snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs13358657
rs13358657
1 5 158511062 intron variant A/G snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs142076278
rs142076278
1 16 51794418 intergenic variant A/G snv 9.5E-03 0.700 1.000 1 2019 2019