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: rs10505380
rs10505380
1 1.000 8 120314234 intron variant A/G snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs114830967
rs114830967
1 1.000 2 115820465 intron variant C/T snv 2.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs116264298
rs116264298
1 1.000 4 67496237 intron variant T/C snv 1.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs116502295
rs116502295
1 1.000 11 128462620 intron variant T/C snv 6.1E-03 7.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs117451620
rs117451620
1 1.000 22 33873469 intron variant C/A snv 1.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs12118495
rs12118495
1 1.000 1 204077651 intron variant C/T snv 7.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs12232685
rs12232685
1 1.000 18 13437028 intron variant C/T snv 4.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs12539913
rs12539913
1 1.000 7 79143230 intron variant G/A snv 3.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs138288216
rs138288216
1 1.000 3 174250679 intron variant G/T snv 7.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs1394432
rs1394432
1 1.000 2 98279575 intron variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs139465532
rs139465532
1 1.000 20 8348184 intron variant C/G snv 6.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs139840509
rs139840509
1 1.000 18 6953581 intron variant G/A snv 1.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs140255439
rs140255439
1 1.000 17 2638960 intron variant C/T snv 6.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs142630661
rs142630661
1 1.000 11 71794579 non coding transcript exon variant C/G snv 1.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs142897541
rs142897541
1 1.000 2 192095144 intron variant C/T snv 1.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs146425640
rs146425640
1 1.000 11 19823052 intron variant A/C snv 2.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs149325996
rs149325996
1 1.000 18 79735872 non coding transcript exon variant G/A snv 1.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs150859230
rs150859230
1 1.000 1 216675108 intron variant C/T snv 1.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs151068302
rs151068302
1 1.000 9 26883048 intron variant C/T snv 6.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs1790634
rs1790634
1 1.000 18 36419450 intron variant G/A snv 0.58 0.700 1.000 1 2019 2019
dbSNP: rs180822335
rs180822335
1 1.000 10 69950109 intron variant T/C snv 5.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs184429573
rs184429573
1 1.000 12 28504235 intron variant A/C snv 9.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs186555016
rs186555016
1 1.000 1 95161598 intron variant T/C snv 1.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs1882642
rs1882642
1 1.000 2 141104341 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs189131320
rs189131320
1 1.000 1 24951485 intron variant C/G snv 2.3E-03 0.700 1.000 1 2019 2019