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: rs10137343
rs10137343
1 14 22913431 intron variant A/T snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs1015438
rs1015438
1 16 51143606 intron variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs1016162
rs1016162
1 3 102299 regulatory region variant C/T snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs10161821
rs10161821
1 13 85129514 intergenic variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10164820
rs10164820
1 2 100433891 intergenic variant G/C snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs1016678
rs1016678
1 17 37514090 downstream gene variant A/G snv 0.72 0.700 1.000 1 2018 2018
dbSNP: rs10171320
rs10171320
1 2 137928042 intergenic variant A/C snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs10177638
rs10177638
1 2 62659875 intron variant C/T snv 0.69 0.700 1.000 1 2018 2018
dbSNP: rs10183150
rs10183150
1 2 100322655 upstream gene variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10189857
rs10189857
6 1.000 0.080 2 60486100 intron variant A/G snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs10192369
rs10192369
2 2 160524377 intergenic variant G/A snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs10193498
rs10193498
1 2 173229617 intron variant A/C;T snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs10196515
rs10196515
1 2 153383795 intergenic variant C/A snv 0.82 0.700 1.000 1 2018 2018
dbSNP: rs10197780
rs10197780
1 2 62646060 intron variant T/C snv 0.78 0.700 1.000 1 2018 2018
dbSNP: rs1019914
rs1019914
1 7 3672560 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10202535
rs10202535
1 2 102957679 intron variant T/C snv 0.61 0.700 1.000 1 2018 2018
dbSNP: rs10205421
rs10205421
1 2 58070529 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10206657
rs10206657
1 2 232597385 intron variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs10208720
rs10208720
1 2 158609502 intron variant T/G snv 0.83 0.700 1.000 1 2018 2018
dbSNP: rs10211312
rs10211312
1 2 62466982 downstream gene variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1021469
rs1021469
1 12 57814381 intron variant G/A snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs10215015
rs10215015
1 7 14785984 intron variant A/G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs10218999
rs10218999
1 10 31076645 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs10223255
rs10223255
1 5 92705821 intergenic variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs10232276
rs10232276
1 7 126943467 intron variant T/C snv 0.23 0.700 1.000 1 2018 2018