Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
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
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs3747207
PNPLA3
22 43928975 intron variant G/A snv 0.22 7
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs142550358 9 88777772 intron variant CT/- delins 3.9E-02 5
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 5
rs66505542
BUD13
11 116752498 intron variant AA/-;A;AAA delins 5
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5