Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs1864325
MAPT
0.882 0.160 17 45900461 intron variant C/T snv 0.14 5
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 5
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs17690703
MAPT-AS1
0.882 0.160 17 45847931 intron variant C/T snv 0.18 4
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 4
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 3
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 3
rs10445371
MAPT
0.925 0.120 17 45988044 intron variant G/A snv 0.15 3
rs1078268
STH ; MAPT
0.925 0.120 17 45998535 intron variant A/G snv 0.15 3
rs11078925
ZPBP2
0.925 0.160 17 39868955 intron variant T/C snv 0.36 3
rs11870965
ZPBP2
0.925 0.160 17 39873952 intron variant T/A snv 0.40 3
rs12936231
ZPBP2
0.925 0.160 17 39872867 intron variant C/G;T snv 3
rs17571739
MAPT
0.925 0.120 17 45955549 intron variant T/C snv 0.14 3
rs17571809
MAPT
0.925 0.120 17 45957493 intron variant A/G snv 0.14 3
rs17572169
MAPT
0.925 0.120 17 45968608 intron variant C/T snv 0.14 3
rs17577094
KANSL1
0.925 0.120 17 46110126 intron variant A/G snv 0.14 3
rs17690679
SPPL2C ; MAPT-AS1
0.925 0.120 17 45847437 intron variant A/G snv 0.14 3
rs17769490
MAPT-AS1
0.925 0.120 17 45848239 intron variant G/A snv 0.14 3
rs17769552
MAPT-AS1
0.925 0.120 17 45849924 intron variant G/A snv 0.14 3
rs199515
WNT3 ; LRRC37A2
0.925 0.120 17 46779275 intron variant G/C snv 0.84 3
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 3
rs3816470
IKZF3
0.925 0.160 17 39829548 intron variant A/G snv 0.54 3