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
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
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
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
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
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
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs35158985
CDH1
0.882 0.080 16 68762843 intron variant A/G snv 0.38 6
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 6
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 6
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5