Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2072183
NPC1L1
0.925 0.040 7 44539581 synonymous variant G/A;C snv 4.0E-06; 0.25 3
rs10094715 0.925 0.040 8 46473341 intergenic variant A/G snv 9.8E-03 2
rs135851
C22orf34
0.925 0.040 22 49583909 intron variant A/C snv 4.4E-02 2
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs9906298
CA10
0.925 0.040 17 51702890 intron variant T/C snv 9.2E-02 2
rs2013647
ZNF28
0.925 0.040 19 52827416 intron variant C/T snv 0.11 2
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 4
rs17066440 0.925 0.040 18 59981043 intergenic variant T/C snv 3.3E-02 2
rs1475029
LOC729296 ; MIR646HG
0.925 0.040 20 60093953 intron variant A/G snv 0.23 2
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs8083296
L3MBTL4
0.925 0.040 18 6158717 intron variant A/C snv 5.4E-02 2
rs2241423
MAP2K5
0.882 0.120 15 67794500 intron variant G/A snv 0.29 2
rs2865108 0.925 0.040 7 67861752 intergenic variant C/A snv 0.89 2
rs10998022
MYPN
0.925 0.040 10 68210229 intron variant C/T snv 0.26 2
rs17088392
DACH1
0.925 0.040 13 71683104 intron variant T/C snv 8.5E-02 2
rs12362105 0.925 0.040 11 76739864 intergenic variant G/A;T snv 2
rs17063627
GNA14
0.925 0.040 9 77424742 intron variant A/G snv 7.2E-02 2
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 1
rs11186149
SH2D4B
0.925 0.040 10 80580951 intron variant T/C snv 8.6E-02 2
rs8061765
TMEM114
0.925 0.040 16 8540871 intron variant G/A snv 0.11 2
rs12314274 0.925 0.040 12 85855418 intergenic variant T/C snv 0.37 2
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 2