Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17563986
MAPT
1.000 0.040 17 45913906 intron variant A/G snv 0.14 3
rs1981997
MAPT
1.000 0.040 17 45979401 non coding transcript exon variant G/A snv 0.14 3
rs10445338
MAPT
1.000 0.040 17 45990316 intron variant G/A snv 0.15 2
rs17564983
LOC105371800 ; MAPT
1.000 0.040 17 45934459 intron variant A/C snv 0.14 2
rs17573175
MAPT
1.000 0.040 17 45993723 intron variant C/G;T snv 2
rs17691610
MAPT ; MAPT-AS1
1.000 0.040 17 45893296 intron variant G/T snv 0.14 2
rs17770343
MAPT-AS1 ; MAPT
1.000 0.040 17 45892788 intron variant T/C snv 0.14 2
rs1991556
MAPT
1.000 0.040 17 46006036 intron variant G/A snv 0.14 2
rs1052551
MAPT
1.000 0.040 17 45991558 synonymous variant G/A;T snv 0.14; 8.0E-05 1
rs17563965
MAPT
1.000 0.040 17 45913553 intron variant A/G snv 0.14 1
rs4792891
MAPT ; MAPT-AS1 ; MAPT-IT1
1.000 0.040 17 45896132 non coding transcript exon variant T/G snv 0.30 1
rs2435200
MAPT
0.925 0.080 17 45994485 intron variant G/A snv 0.40 1
rs7521
MAPT ; KANSL1
0.925 0.080 17 46028029 3 prime UTR variant A/C;G snv 1
rs9468
MAPT
0.882 0.080 17 46024197 3 prime UTR variant T/C snv 0.15 0.14 1
rs10445337
MAPT
0.925 0.120 17 45990034 missense variant T/C snv 0.15 0.15 3
rs1052587
MAPT
0.925 0.120 17 46025238 3 prime UTR variant T/C snv 0.14 3
rs1078268
STH ; MAPT
0.925 0.120 17 45998535 intron variant A/G snv 0.15 3
rs17574228
KANSL1 ; MAPT
0.925 0.120 17 46027143 3 prime UTR variant T/C snv 0.14 3
rs17650901
MAPT
0.925 0.120 17 45962325 5 prime UTR variant A/G snv 0.14 0.14 3
rs17652121
MAPT
0.925 0.120 17 45996607 synonymous variant T/C snv 0.14 0.15 3
rs1800547
MAPT
0.925 0.120 17 45974480 non coding transcript exon variant A/G snv 0.15 0.14 3
rs767057
MAPT ; LOC105371800
0.925 0.120 17 45921456 intron variant A/G snv 0.14 3
rs17649641
MAPT ; LOC105371800
0.925 0.120 17 45920006 intron variant T/C snv 0.14 2
rs62063857
STH ; MAPT
0.882 0.120 17 45999299 missense variant A/G snv 0.14 0.15 2
rs1864325
MAPT
0.882 0.160 17 45900461 intron variant C/T snv 0.14 5