Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17690703
MAPT-AS1
0.882 0.160 17 45847931 intron variant C/T snv 0.18 4
rs12373139
MAPT-AS1 ; SPPL2C
0.925 0.120 17 45846764 missense variant G/A snv 0.15 0.14 4
rs199533
NSF ; LRRC37A2
0.925 0.120 17 46751565 synonymous variant G/A snv 0.13 0.13 4
rs12185233
SPPL2C ; MAPT-AS1
0.882 0.160 17 45846288 missense variant G/A;C snv 9.5E-05; 0.15 4
rs12373123
SPPL2C ; MAPT-AS1
0.882 0.160 17 45846707 missense variant T/C snv 0.15 0.14 4
rs12373142
SPPL2C ; MAPT-AS1
0.851 0.200 17 45846834 missense variant C/G;T snv 0.15 4
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs11557467
ZPBP2
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45 4
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs12950743 0.925 0.160 17 39892980 intergenic variant T/C snv 0.45 3
rs2006996 0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 3
rs715412 1.000 0.080 11 118813901 regulatory region variant G/A snv 0.17 3
rs7359623 0.925 0.160 17 39893336 intergenic variant C/T snv 0.44 3
rs9901146 0.882 0.160 17 39887090 intergenic variant G/A snv 0.45 3
rs9907088 0.925 0.160 17 39878863 downstream gene variant G/A snv 0.39 3
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 3
rs7224129
GSDMB
0.925 0.160 17 39919173 non coding transcript exon variant G/A snv 0.52 3
rs869402
GSDMB
0.925 0.160 17 39911790 intron variant T/A;C snv 3
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 3
rs3816470
IKZF3
0.925 0.160 17 39829548 intron variant A/G snv 0.54 3
rs907091
IKZF3
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47 3
rs9909593
IKZF3
0.925 0.160 17 39813896 intron variant A/G snv 0.38 3