Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 7
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11 6
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs17410962 1.000 0.040 8 19990569 intergenic variant G/A snv 0.15 6
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 6
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 5
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 5
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 4
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs11722228
SLC2A9
0.851 0.160 4 9914117 intron variant C/T snv 0.32 4
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 4
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 4