Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs10116277
CDKN2B-AS1
0.827 0.160 9 22081398 intron variant G/T snv 0.62 5
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 5
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 5
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 5
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 5
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs523096
CDKN2B-AS1
0.827 0.080 9 22019130 intron variant A/G snv 0.30 5
rs6475606
CDKN2B-AS1
0.882 0.080 9 22081851 intron variant C/T snv 0.62 5
rs7049105
CDKN2B-AS1
0.807 0.120 9 22028802 intron variant A/G snv 0.58 5
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 4
rs10965219
CDKN2B-AS1
0.882 0.080 9 22053688 intron variant A/G snv 0.58 4
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 4
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 4
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 4
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 4
rs1537375
CDKN2B-AS1
0.882 0.120 9 22116072 intron variant T/C;G snv 4
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 4
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 4
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 4
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14 4
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 4