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: rs34923414
rs34923414
1 22 28820734 intron variant C/T snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs117107603
rs117107603
1 7 149564734 intron variant C/A snv 1.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs11671654
rs11671654
1 19 11903540 intron variant C/G snv 0.46 0.37 0.700 1.000 1 2019 2019
dbSNP: rs2072153
rs2072153
3 17 49312652 intron variant G/A;C snv 3.7E-04; 0.33 0.700 1.000 1 2019 2019
dbSNP: rs12478953
rs12478953
1 2 71391469 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs74789101
rs74789101
1 19 12609925 missense variant G/A snv 5.9E-02 5.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs151305716
rs151305716
3 20 53605567 intron variant C/T snv 8.1E-03 0.700 1.000 2 2016 2019
dbSNP: rs56408111
rs56408111
1 19 19682736 3 prime UTR variant T/C snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs697248
rs697248
1 10 79044959 intron variant G/C snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs7641761
rs7641761
1 3 179022634 3 prime UTR variant T/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs187673688
rs187673688
1 7 99529193 intron variant T/G snv 3.6E-03 0.700 1.000 1 2019 2019
dbSNP: rs142529006
rs142529006
4 7 100022093 intron variant T/A snv 6.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs1007934
rs1007934
3 14 72996771 intron variant G/A snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs12232375
rs12232375
2 16 88500003 intron variant G/A;C;T snv 0.700 1.000 2 2016 2019
dbSNP: rs149290349
rs149290349
3 2 43224818 missense variant G/A;T snv 6.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs34074875
rs34074875
1 8 134640328 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs10210063
rs10210063
1 2 144425390 intron variant C/G snv 7.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs62410539
rs62410539
3 3 196197165 downstream gene variant C/T snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs2492301
rs2492301
4 1 37473572 intron variant T/C snv 0.53 0.700 1.000 2 2016 2019
dbSNP: rs10415135
rs10415135
3 19 4061546 intron variant C/T snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs56356382
rs56356382
3 19 4064059 intron variant T/C snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs6062322
rs6062322
1 20 63810246 intron variant A/C;T snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs4902288
rs4902288
1 14 64516222 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs17116384
rs17116384
3 11 114110519 intron variant A/G snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs142267802
rs142267802
ZAN
1 7 100743255 intron variant C/T snv 1.9E-02 0.700 1.000 1 2019 2019