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: rs10501320
rs10501320
5 0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs11039391
rs11039391
1 11 47775110 downstream gene variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11665052
rs11665052
1 18 60241442 intergenic variant A/G snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs12787112
rs12787112
1 11 47665595 intron variant A/G snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs17093914
rs17093914
2 1.000 0.040 14 74896938 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2193596
rs2193596
1 14 74767398 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs34467936
rs34467936
3 1.000 0.040 11 47893747 intergenic variant A/G snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs35344466
rs35344466
1 3 85583871 intron variant A/C snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs62081501
rs62081501
4 0.925 0.080 18 37627749 intron variant G/A snv 6.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs6478623
rs6478623
2 1.000 0.040 9 123552844 intron variant T/G snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs7611991
rs7611991
1 3 85710408 intron variant G/A snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs9854869
rs9854869
2 1.000 0.040 3 85371574 intron variant C/A snv 0.17 0.700 1.000 1 2018 2018