Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10218795
HJV
1.000 0.040 1 146018957 intron variant G/A snv 0.15 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 1
rs12091564 1.000 0.040 1 146039391 upstream gene variant A/C;G snv 1
rs1614866 1.000 0.040 1 211527316 regulatory region variant G/A snv 7.1E-02 1
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 1
rs17114046
PLPP3
0.925 0.040 1 56500678 intron variant A/G snv 0.12 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 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
rs2133189
MIA3
0.925 0.040 1 222641100 intron variant C/T snv 0.56 1
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 1
rs2291832
MIA3
1.000 0.040 1 222653139 intron variant G/A;C snv 0.64; 1.2E-05 1
rs2404715
PLPP3
1.000 0.040 1 56543106 intron variant C/T snv 7.6E-02 1
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 1
rs3931020 0.882 0.040 1 74769633 downstream gene variant T/C snv 0.71 1
rs4846049
C1orf167 ; MTHFR
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 1
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 1
rs7553007 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6