Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 3
rs5996074
SREBF2
22 41840333 intron variant G/A snv 0.74 3
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 2
rs11065756
CCDC63
0.925 0.080 12 110900990 intron variant C/T snv 6.1E-02 2
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59 2
rs151181
CLN3
1.000 0.040 16 28479196 intron variant T/C snv 0.32 2
rs2238149
CCDC63
1.000 0.040 12 110874125 intron variant T/C snv 0.33 2
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32 2
rs3781264
PLCE1
0.851 0.120 10 94310618 intron variant A/G snv 0.25 2
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 2
rs4851005
IL18R1
2 102395092 intron variant C/T snv 0.29 2
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 2
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv 2
rs1000668
TMC1
9 72790943 intron variant T/A;G snv 1
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 1
rs10058728
CSNK1A1
1.000 0.080 5 149524529 intron variant A/T snv 0.64 1
rs10186527
FLACC1
2 201335852 intron variant C/T snv 0.54 1
rs10191793
ST6GAL2
2 106809420 intron variant A/G snv 0.21 1
rs10197246
FLACC1
2 201340018 intron variant T/C snv 0.72 1
rs10201587
FLACC1
2 201338068 intron variant A/G snv 0.47 1
rs10274928
JAZF1
7 28102469 intron variant A/G;T snv 1
rs10454127
FLACC1
2 201347651 intron variant G/A;T snv 1