Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11186149
SH2D4B
0.925 0.040 10 80580951 intron variant T/C snv 8.6E-02 2
rs41506144
FRMD4A
0.925 0.040 10 13834687 intron variant C/G;T snv 2
rs12362105 0.925 0.040 11 76739864 intergenic variant G/A;T snv 2
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs12314274 0.925 0.040 12 85855418 intergenic variant T/C snv 0.37 2
rs2384506 0.851 0.080 12 114991548 intergenic variant T/C snv 0.21 2
rs4149000
SLCO1A2
0.882 0.080 12 21295063 non coding transcript exon variant C/T snv 0.11 2
rs17088392
DACH1
0.925 0.040 13 71683104 intron variant T/C snv 8.5E-02 2
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 1
rs2241423
MAP2K5
0.882 0.120 15 67794500 intron variant G/A snv 0.29 2
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4
rs8061765
TMEM114
0.925 0.040 16 8540871 intron variant G/A snv 0.11 2
rs9906298
CA10
0.925 0.040 17 51702890 intron variant T/C snv 9.2E-02 2
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs17066440 0.925 0.040 18 59981043 intergenic variant T/C snv 3.3E-02 2
rs8083296
L3MBTL4
0.925 0.040 18 6158717 intron variant A/C snv 5.4E-02 2
rs2013647
ZNF28
0.925 0.040 19 52827416 intron variant C/T snv 0.11 2
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 5
rs1475029
LOC729296 ; MIR646HG
0.925 0.040 20 60093953 intron variant A/G snv 0.23 2
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs135851
C22orf34
0.925 0.040 22 49583909 intron variant A/C snv 4.4E-02 2
rs738785
GUSBP11
0.925 0.040 22 23680444 intron variant C/T snv 0.49 2