Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 3
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 3
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 3
rs944801
CDKN2B-AS1
0.882 0.120 9 22051671 intron variant G/A;C snv 3
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 3
rs10211524
LOC107984063 ; LINC02245
2 64980940 intron variant G/A snv 0.51 3
rs10978777 1.000 0.080 9 107268309 intergenic variant G/A;C snv 2
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs11509197 1.000 0.080 7 118641356 intergenic variant C/T snv 0.38 2
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs1481805 1.000 0.080 8 71121190 intron variant A/T snv 0.58 2
rs6506897 1.000 0.080 18 31215320 intergenic variant G/A snv 0.62 2
rs73169578 1.000 0.080 13 21120420 intergenic variant G/A snv 3.1E-02 2
rs74155456 1.000 0.080 10 61070020 intergenic variant T/C snv 2.3E-02 2
rs74910095 1.000 0.080 5 63545132 intergenic variant T/A snv 3.7E-02 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
rs77934287 1.000 0.080 12 23071319 intron variant A/G;T snv 2
rs9641609 1.000 0.080 7 118657790 regulatory region variant A/G snv 0.38 2
rs72928364
ABI3BP
1.000 0.080 3 100894935 intron variant C/T snv 0.39 2
rs7804216
ACTR3C
1.000 0.080 7 149941248 intergenic variant C/G snv 0.24 2
rs6898559
ALDH7A1
1.000 0.080 5 126557237 intron variant G/A snv 0.66 2
rs74570061
ARL9
1.000 0.080 4 56517605 intron variant T/C snv 3.9E-02 2
rs16879003
ATXN1
1.000 0.080 6 16745008 intron variant T/C;G snv 2