Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 3
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 2
rs12405132
RNF115
0.882 0.200 1 145790097 intron variant G/A snv 0.29 2
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 2
rs4245739
MDM4
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 2
rs4971059
TRIM46
0.851 0.200 1 155176305 intron variant G/A snv 0.34 2
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 1
rs11552449
AP4B1 ; DCLRE1B
0.925 0.080 1 113905767 missense variant C/G;T snv 0.22 0.15 1
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs2290854
MDM4
0.925 0.080 1 204546897 intron variant A/G snv 0.65 0.57 1
rs2494251 0.925 0.080 1 159311361 downstream gene variant G/A;C snv 1
rs616488
PEX14
0.925 0.080 1 10506158 intron variant A/G snv 0.27 1
rs6678914
LGR6
0.882 0.080 1 202218048 intron variant G/A snv 0.37 1
rs6682208
LOC105371692
1.000 0.080 1 204597055 intergenic variant T/C snv 0.56 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 1
rs844648
TNFSF4 ; LOC100506023
0.807 0.280 1 173254724 regulatory region variant G/A snv 0.46 1
rs903263
LOC107985046 ; PRKACB
1.000 0.080 1 84156830 intron variant G/A;T snv 1
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6