Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs1412834
CDKN2B-AS1
0.790 0.080 9 22110132 intron variant T/C snv 0.64 11
rs7865618
CDKN2B-AS1
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 11
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs1333047
CDKN2B-AS1
0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs10116277
CDKN2B-AS1
0.827 0.160 9 22081398 intron variant G/T snv 0.62 8
rs751093906
SLC20A2
0.882 0.200 8 42472255 stop gained G/A;C snv 4.0E-06 8
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 7
rs10120688
CDKN2B-AS1
0.807 0.080 9 22056500 intron variant G/A snv 0.50 7
rs10811656
CDKN2B-AS1
0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs523096
CDKN2B-AS1
0.827 0.080 9 22019130 intron variant A/G snv 0.30 7
rs7049105
CDKN2B-AS1
0.807 0.120 9 22028802 intron variant A/G snv 0.58 7
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 6
rs1537375
CDKN2B-AS1
0.882 0.120 9 22116072 intron variant T/C;G snv 6
rs2383204
CDKN2B-AS1
0.827 0.160 9 22055049 intron variant A/G;T snv 6
rs496892
CDKN2B-AS1
0.827 0.160 9 22024352 intron variant C/T snv 0.40 6
rs634537
CDKN2B-AS1
0.851 0.080 9 22032153 intron variant T/G snv 0.28 6
rs9632884
CDKN2B-AS1
0.851 0.160 9 22072302 intron variant G/A;C snv 6
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 6
rs2026458
PHACTR1
0.882 0.080 6 12825642 intron variant C/T snv 0.34 6
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 6
rs10738610
CDKN2B-AS1
0.882 0.120 9 22123767 intron variant A/C;T snv 5
rs10811650
CDKN2B-AS1
0.882 0.200 9 22067594 intron variant A/G snv 0.37 5