Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111269058 7 73561372 upstream gene variant C/T snv 9.8E-02 1
rs12029262 1 159709406 upstream gene variant G/C snv 8.5E-02 1
rs12568139 1 19985183 upstream gene variant A/G snv 6.0E-02 1
rs1441169
LINC01953 ; LOC105373864
2 213168806 upstream gene variant A/C;G snv 1
rs16842559 1 159706381 upstream gene variant T/C snv 5.6E-02 1
rs1874467
LOC107984887
16 51056690 upstream gene variant C/G snv 0.13 1
rs2233688
PLA2G2E
1 19924237 upstream gene variant A/G snv 0.16 1
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 1
rs2808628 1 159706221 upstream gene variant G/A snv 0.31 1
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 1
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 1
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 1
rs55855238 18 57422483 upstream gene variant T/C snv 0.46 1
rs9271608 6 32623811 upstream gene variant A/G snv 0.15 1
rs7953249
HNF1A-AS1
0.882 0.160 12 120965921 splice region variant G/A snv 0.59 4
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 2
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 1
rs34931250
ABCA8
17 68883786 splice region variant C/T snv 3.8E-02 3.7E-02 1
rs2858310 1.000 0.120 6 32700546 TF binding site variant G/A snv 0.64 2
rs4131568 1 159752266 TF binding site variant C/T snv 0.26 1
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 10
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 7
rs1892534
LEPR
0.925 0.120 1 65640261 3 prime UTR variant C/T snv 0.44 3
rs1127311
ADAR ; CHRNB2
1 154584187 3 prime UTR variant G/A snv 0.42 2