Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16879003
ATXN1
1.000 0.080 6 16745008 intron variant T/C;G snv 2
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs2680830
VSNL1
1.000 0.080 2 17596817 intron variant A/G;T snv 0.94 2
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 6
rs6754498
LOC107985783
1.000 0.080 2 185953121 non coding transcript exon variant A/C;G;T snv 2
rs1912826
KLKB1
4 186228386 intron variant G/A;C snv 4
rs712964 22 19168604 upstream gene variant T/C snv 0.66 2
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs73169578 1.000 0.080 13 21120420 intergenic variant G/A snv 3.1E-02 2
rs3218020
CDKN2B-AS1
0.882 0.120 9 21997873 intron variant G/A;C snv 5
rs3217992
CDKN2B-AS1 ; CDKN2B
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs2069418
CDKN2B-AS1 ; CDKN2B
1.000 0.040 9 22009699 intron variant G/C snv 0.70 2
rs2069416
CDKN2B ; CDKN2B-AS1
0.925 0.040 9 22010005 intron variant T/A;G snv 3
rs10811641
CDKN2B-AS1
1.000 0.040 9 22014138 non coding transcript exon variant C/G snv 0.32 2
rs2106120
CDKN2B-AS1
1.000 0.040 9 22017102 intron variant G/T snv 0.56 2
rs2106119
CDKN2B-AS1
1.000 0.040 9 22017551 intron variant A/G;T snv 2
rs7044859
CDKN2B-AS1
0.925 0.080 9 22018782 intron variant T/A snv 0.56 3
rs523096
CDKN2B-AS1
0.827 0.080 9 22019130 intron variant A/G snv 0.30 7
rs10757264
CDKN2B-AS1
1.000 0.040 9 22019733 intron variant A/G snv 0.58 2
rs10965212
CDKN2B-AS1
0.925 0.080 9 22023796 intron variant T/A;C;G snv 3
rs496892
CDKN2B-AS1
0.827 0.160 9 22024352 intron variant C/T snv 0.40 6
rs10811643
CDKN2B-AS1
1.000 0.040 9 22024967 intron variant A/G snv 0.56 2
rs10738604
CDKN2B-AS1
1.000 0.040 9 22025494 intron variant G/A snv 0.29 3