Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 4
rs11057830
SCARB1
0.851 0.040 12 124822507 intron variant G/A snv 0.15 4
rs12801636
PCNX3
1.000 0.040 11 65623846 intron variant G/A snv 0.25 4
rs1748195
DOCK7
0.851 0.120 1 62583922 intron variant C/G;T snv 4
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 4
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 4
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 4
rs10738607
CDKN2B-AS1
0.925 0.080 9 22088095 intron variant A/G snv 0.42 3
rs10811652
CDKN2B-AS1
0.882 0.120 9 22077086 intron variant A/C;T snv 3
rs11024074
PLEKHA7
0.925 0.040 11 16895672 intron variant T/C snv 0.29 3
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 3
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 3
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 3
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 3
rs12133641
IL6R
0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs12500824
SHROOM3
1.000 0.040 4 76495474 intron variant A/G;T snv 3
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 3
rs140570886
LPA
1.000 0.040 6 160591981 intron variant T/C snv 2.8E-02 3
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 3
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 3
rs1591805
CENPW
1.000 0.040 6 126395918 intron variant A/G snv 0.47 3
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 3
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 3
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 3