Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 15
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 10
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 9
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6