Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2160669
ZPR1
1.000 0.040 11 116776891 3 prime UTR variant C/T snv 0.92 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11 6
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs603446
ZPR1
1.000 0.040 11 116783719 intron variant C/T snv 0.33 1
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 7
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 1
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 6
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs11600380 1.000 0.040 11 116799466 intergenic variant T/C snv 6.6E-02 2
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 1
rs675
APOA4
1.000 0.040 11 116820959 missense variant T/A;C snv 0.15; 1.2E-03 1
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 1
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs7865146 1.000 0.040 9 127857358 upstream gene variant C/G;T snv 1
rs6947830 0.925 0.080 7 15025359 intergenic variant G/A;C snv 2
rs5945326 0.925 0.080 X 153634467 regulatory region variant A/G snv 0.25 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs2108622
CYP4F2
0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 2