Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811650
CDKN2B-AS1
0.882 0.200 9 22067594 intron variant A/G snv 0.37 5
rs2891168
CDKN2B-AS1
0.851 0.160 9 22098620 intron variant A/G snv 0.40 5
rs10738607
CDKN2B-AS1
0.925 0.080 9 22088095 intron variant A/G snv 0.42 4
rs10965219
CDKN2B-AS1
0.882 0.080 9 22053688 intron variant A/G snv 0.58 4
rs1537378
CDKN2B-AS1
0.882 0.160 9 22061615 intron variant A/G snv 0.73 4
rs10757279
CDKN2B-AS1
0.925 0.040 9 22124631 intron variant A/G snv 0.40 3
rs1537374
CDKN2B-AS1
1.000 0.040 9 22116047 intron variant A/G snv 0.64 3
rs10115049
CDKN2B-AS1
1.000 0.040 9 22032120 intron variant A/G snv 0.46 2
rs10757264
CDKN2B-AS1
1.000 0.040 9 22019733 intron variant A/G snv 0.58 2
rs10757277
CDKN2B-AS1
1.000 0.040 9 22124451 intron variant A/G snv 0.40 2
rs10811643
CDKN2B-AS1
1.000 0.040 9 22024967 intron variant A/G snv 0.56 2
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs16850360 4 74006728 intron variant A/G snv 4.2E-02 2
rs3798722
ELOVL2
6 11040190 intron variant A/G snv 0.39 2
rs4272321
PTPRN2
1.000 0.080 7 158159143 intron variant A/G snv 4.6E-04 2
rs76294234 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 2
rs7689240 1.000 0.080 4 35313869 intergenic variant A/G snv 0.21 2
rs7866783
CDKN2B-AS1
1.000 0.040 9 22056360 non coding transcript exon variant A/G snv 0.71 2
rs944799
CDKN2B-AS1
1.000 0.040 9 22050614 intron variant A/G snv 0.50 2
rs9641609 1.000 0.080 7 118657790 regulatory region variant A/G snv 0.38 2
rs10502575 18 31756628 downstream gene variant A/G snv 6.9E-02 1
rs2168889 4 74357994 intergenic variant A/G snv 4.7E-02 1
rs2390582
LOC105378851
1 90478350 intergenic variant A/G snv 0.15 1
rs7341791
CDKN2B-AS1
9 22112428 intron variant A/G snv 0.65 1