Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 1
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 1
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 1
rs7088058
PLEKHA1
0.851 0.040 10 122389836 intron variant C/T snv 0.32 1
rs767455
TNFRSF1A
0.742 0.400 12 6341779 synonymous variant T/C snv 0.37 0.40 1
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 1
rs1020388 5 56264200 upstream gene variant T/G snv 0.34 2
rs10932019 2 203764087 downstream gene variant G/A;C snv 2
rs1355208 2 30222456 intergenic variant A/G snv 0.65 2
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 2
rs2155433 11 118742212 intron variant G/A snv 0.24 2
rs4626515 7 140204330 intergenic variant T/C snv 0.22 2
rs636393 6 137686393 intron variant G/T snv 0.66 2
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 2
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 2
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 2
rs906868 0.925 0.120 2 30225478 intergenic variant G/T snv 0.53 2
rs975730 8 128303768 intergenic variant G/A snv 0.45 2
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 2
rs229541
C1QTNF6
0.807 0.200 22 37195278 intron variant G/A snv 0.49 2
rs4077515
CARD9
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 2
rs10892286
DDX6
11 118771376 intron variant A/C snv 0.17 2
rs11984075
ELMO1
7 37397251 intron variant A/G snv 0.14 2
rs1772408
IFI16
1 159035859 intron variant A/G;T snv 2