Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 2
rs4654748
NBPF3
1.000 0.040 1 21459575 intron variant C/T snv 0.38 2
rs4657175
NOS1AP
1.000 0.040 1 162225948 intron variant T/C;G snv 2
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 2
rs10429924 1.000 0.040 1 244227262 intergenic variant C/T snv 8.8E-02 1
rs10489202
MPC2
0.925 0.080 1 167933841 intron variant G/T snv 0.20 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs10789369 1.000 0.040 1 73359226 downstream gene variant A/G;T snv 1
rs11165389 1.000 0.040 1 95350307 downstream gene variant T/G snv 0.33 1
rs1198588 1.000 0.040 1 98087276 intergenic variant A/T snv 0.78 1
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 1
rs12071951 1.000 0.040 1 96648359 intergenic variant T/G snv 0.27 1
rs12140439 1.000 0.040 1 177753772 intron variant C/A snv 0.24 1
rs12732868 1.000 0.040 1 5274577 regulatory region variant T/G snv 6.0E-02 1
rs14403
AKT3 ; SDCCAG8
1.000 0.040 1 243500591 3 prime UTR variant C/T snv 0.17 1
rs1538774
SDCCAG8
1.000 0.040 1 243381525 intron variant C/G snv 0.78 1
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 1
rs3027001
CADM3-AS1 ; CADM3
1.000 0.040 1 159199673 intron variant C/G;T snv 1