Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 5
rs10994397
ANK3
0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 5
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 5
rs2799573
CACNB2
0.851 0.040 10 18312999 intron variant T/C snv 0.20 5
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 5
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 5
rs190065944
CHRNA5
0.925 0.080 15 78567268 intron variant G/A snv 3.4E-03 5
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 5
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs12325410
LOC101927026
0.851 0.040 16 9581389 intron variant T/G snv 0.16 5
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 5
rs7004633
LOC105375630
0.851 0.040 8 88748082 intron variant A/G snv 0.28 5
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5