Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs591120
CRYZL2P-SEC16B ; SEC16B
1 177933618 missense variant G/A;C snv 4.0E-06; 0.42 2
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 5
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 3
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 3
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 3
rs13034723
C2orf88
2 190120954 intron variant G/A snv 0.37 2
rs12444979
LOC105371116
1.000 0.080 16 19922278 intergenic variant C/T snv 0.11 2
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 2
rs12597579 16 20246545 intergenic variant C/A;T snv 2
rs9368219
CDKAL1
1.000 0.080 6 20674460 intron variant C/T snv 0.19 3
rs9356744
CDKAL1
0.882 0.120 6 20685255 intron variant T/C snv 0.42 3
rs7766070
CDKAL1
1.000 0.080 6 20686342 intron variant C/A snv 0.25 3
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs2206734
CDKAL1
0.882 0.160 6 20694653 intron variant C/T snv 0.20 3
rs7800783
DNAH11
7 21731847 intron variant G/A snv 5.9E-02 2
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs7374732 1.000 0.080 3 23161963 regulatory region variant C/T snv 0.73 1
rs7586879
ADCY3
2 24894108 intron variant C/T snv 0.47 2
rs6545814
ADCY3
2 24908447 intron variant A/G snv 0.53 2
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 2
rs713586 0.925 0.160 2 24935139 intergenic variant T/C snv 0.58 2
rs1561288
EFR3B
2 25146133 3 prime UTR variant C/T snv 0.29 2
rs12999687
DNMT3A
2 25289569 intron variant T/G snv 0.48 2
rs10261878 7 25910925 intergenic variant A/C snv 0.80 2