Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs469772 1 91064748 intergenic variant C/T snv 0.19 2
rs75460349
ZDHHC18
1 26853597 intron variant A/C snv 1.7E-02 2
rs10494326 1 159679910 intergenic variant C/T snv 5.3E-02 1
rs10889569
LEPR
1 65620511 intron variant A/T snv 0.46 1
rs10925027
NLRP3 ; OR2B11
1 247449260 3 prime UTR variant T/C snv 0.58 1
rs11265191
OR10J1 ; OR10J4
1 159430569 intron variant C/G;T snv 1
rs11265260 1.000 0.080 1 159730249 intergenic variant A/G snv 6.8E-02 1
rs11265263 1 159740727 intergenic variant C/A;T snv 1
rs11573260
PLA2G5
1 20083047 intron variant C/T snv 8.1E-03 1
rs12023742 1 19965513 intergenic variant C/A;G snv 1
rs12029262 1 159709406 upstream gene variant G/C snv 8.5E-02 1
rs12034383
CR1
1 207630250 intron variant G/A snv 0.47 1
rs12034598
CR1
1 207584170 intron variant A/G snv 0.19 1
rs12037222 1 39599289 regulatory region variant G/A snv 0.16 1
rs12083537
IL6R
0.882 0.200 1 154408627 intron variant A/G snv 0.22 1
rs12093699 1 159678198 intergenic variant G/A;C snv 0.31 1
rs12408941 1 19958994 intergenic variant G/A snv 9.7E-02 1
rs12568139 1 19985183 upstream gene variant A/G snv 6.0E-02 1
rs12722987 1 20128727 intergenic variant C/A snv 0.17 1
rs12749227 1 159689319 intergenic variant C/T snv 0.25 1
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 1
rs13375019 1 65657453 intergenic variant G/C;T snv 1
rs13375942 1 19965885 regulatory region variant T/A;C;G snv 1
rs1341665 1.000 0.080 1 159721769 intergenic variant G/A snv 0.32 1
rs149520992 1 159697727 intergenic variant C/T snv 3.8E-03 1