Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4712523
CDKAL1
0.925 0.120 6 20657333 intron variant A/G snv 0.41 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 3
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 3
rs12518099
LINC01339
0.925 0.120 5 90250292 intron variant A/G;T snv 3
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs4689388
WFS1
0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64 3
rs11894266 1.000 0.080 2 169780132 downstream gene variant C/T snv 0.45 2
rs2582367 1.000 0.080 8 27622508 regulatory region variant C/T snv 0.64 2
rs543293 0.925 0.080 11 86109035 regulatory region variant A/G snv 0.72 2
rs8103315
BCL3
1.000 0.080 19 44750911 intron variant C/A snv 9.1E-02 2
rs3760627
CLPTM1
1.000 0.080 19 44953923 non coding transcript exon variant T/C snv 0.80 0.51 2
rs12610605
NECTIN2
1.000 0.080 19 44867581 intron variant G/A snv 0.15 2
rs1871047
NECTIN2
1.000 0.080 19 44848489 intron variant A/G snv 0.31 2
rs377702
NECTIN2
1.000 0.080 19 44859410 intron variant G/A snv 0.34 2
rs1048699
PPP1R37 ; MARK4
1.000 0.080 19 45147128 3 prime UTR variant C/T snv 9.0E-02 2
rs1114832
PPP1R37 ; MARK4
1.000 0.080 19 45132943 intron variant C/T snv 9.2E-02 2
rs7941541 11 86147496 intergenic variant G/A snv 0.73 1
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 1
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 1
rs689
INS ; INS-IGF2
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 1
rs7171171
LOC107984725
0.925 0.120 15 38614840 intergenic variant A/G snv 0.24 1
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 1