Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4953023
ABCG8
0.925 0.040 2 43846861 non coding transcript exon variant G/A snv 6.9E-02 5
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
rs1011770
BAZ2B
0.925 0.040 2 159382207 intron variant A/G snv 2.5E-02 2
rs10888095
SGCZ
0.925 0.040 8 15004905 intron variant C/A;G snv 2
rs10998022
MYPN
0.925 0.040 10 68210229 intron variant C/T snv 0.26 2
rs11186149
SH2D4B
0.925 0.040 10 80580951 intron variant T/C snv 8.6E-02 2
rs12314274 0.925 0.040 12 85855418 intergenic variant T/C snv 0.37 2
rs12362105 0.925 0.040 11 76739864 intergenic variant G/A;T snv 2
rs135851
C22orf34
0.925 0.040 22 49583909 intron variant A/C snv 4.4E-02 2
rs1475029
LOC729296 ; MIR646HG
0.925 0.040 20 60093953 intron variant A/G snv 0.23 2
rs16824658
HMCN1
0.925 0.040 1 185895380 intron variant A/G snv 7.6E-02 2
rs16843641
TANC1
0.925 0.040 2 159061866 intron variant T/C snv 1.2E-02 2
rs17063627
GNA14
0.925 0.040 9 77424742 intron variant A/G snv 7.2E-02 2
rs17066440 0.925 0.040 18 59981043 intergenic variant T/C snv 3.3E-02 2
rs17088392
DACH1
0.925 0.040 13 71683104 intron variant T/C snv 8.5E-02 2
rs17241442
TNC ; DELEC1
0.925 0.040 9 115062806 intron variant G/A snv 0.11 2
rs2013647
ZNF28
0.925 0.040 19 52827416 intron variant C/T snv 0.11 2
rs253314
MYO10
0.925 0.040 5 16871155 intron variant A/C snv 6.9E-02 2
rs2865108 0.925 0.040 7 67861752 intergenic variant C/A snv 0.89 2
rs41440452 0.925 0.040 9 122717961 intergenic variant G/A snv 7.9E-02 2
rs41506144
FRMD4A
0.925 0.040 10 13834687 intron variant C/G;T snv 2
rs6598902
STX12
0.925 0.040 1 27779198 intron variant T/C snv 0.18 2
rs738785
GUSBP11
0.925 0.040 22 23680444 intron variant C/T snv 0.49 2
rs8061765
TMEM114
0.925 0.040 16 8540871 intron variant G/A snv 0.11 2