Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs7947761
ARHGAP42
1.000 0.040 11 100753868 intron variant A/G snv 0.26 1
rs4754698
ARHGAP42
1.000 0.040 11 100761177 intron variant C/A;G snv 1
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 1
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 5
rs4919687
CYP17A1
0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 9
rs11191416
LOC107984264
1.000 0.040 10 102845159 intron variant T/G snv 0.10 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs3740390
AS3MT ; BORCS7-ASMT
0.925 0.080 10 102878723 intron variant C/T snv 9.2E-02 1
rs12788925 1.000 0.040 11 102931118 intergenic variant A/G snv 0.32 1
rs12414777
CNNM2
1.000 0.040 10 102938024 intron variant C/G;T snv 0.20 1
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 2
rs10861032
C12orf42
0.925 0.040 12 103518728 non coding transcript exon variant T/C snv 0.24 1
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 2
rs2128739 0.925 0.080 11 103802549 intron variant A/C snv 0.68 2
rs2839812 1.000 0.040 11 103802566 intron variant T/A;C snv 1
rs12765878
STN1
0.925 0.160 10 103909864 intron variant T/A;C snv 1
rs4918072 1.000 0.040 10 103933886 regulatory region variant G/A snv 0.28 1
rs28641753 0.925 0.160 3 104256574 intergenic variant C/T snv 4.5E-02 2
rs2472386
ABCA1
1.000 0.040 9 104839260 intron variant G/A snv 0.47 1
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 2
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs17035270 1.000 0.040 4 105115388 intron variant T/C snv 0.20 1
rs2342781
ZFPM2
1.000 0.040 8 105253492 intron variant C/G;T snv 1