Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 6
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 6
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 5
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5
rs74035509
ZFPM1
16 88500925 intron variant C/T snv 0.10 5
rs128494
CLDN14 ; LOC105369301
21 36461960 intron variant T/C snv 0.72 4
rs2337106
SMAD7
18 48934533 intron variant C/A;G snv 4
rs4953318
PRKCE
2 46127912 intron variant A/C snv 0.43 4
rs60695258
AFF1
4 87101557 intron variant C/A;T snv 4
rs10168349
PRKCE
2 46133768 intron variant G/C snv 0.36 3
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 3
rs114948639
PRKCE
2 46066687 intron variant C/T snv 7.2E-03 3
rs115986297
GMDS
6 2050557 intron variant A/C;G snv 3
rs11689538
TFCP2L1
2 121238062 intron variant G/C snv 0.11 3
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 3
rs12811512
GPRC5A
12 12893277 intron variant C/T snv 0.11 3
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10 3
rs17773190
LINC01118
2 46803224 intron variant A/G snv 0.32 3