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
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
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
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5