Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 5
rs11820589
BUD13
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10 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
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs301
LPL
0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 5
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 4
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 4
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 4
rs17489282 1.000 0.040 8 19995007 regulatory region variant C/T snv 0.25 4
rs1919484 1.000 0.040 8 20012165 intergenic variant G/A snv 0.23 4
rs2197089 0.925 0.080 8 19968862 downstream gene variant G/A snv 0.61 4
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 4
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 4
rs6494005
ALDH1A2 ; LIPC
1.000 0.040 15 58432325 non coding transcript exon variant A/G snv 0.38 4
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4