Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 7
rs2869967
FAM13A ; LOC105377327
0.827 0.120 4 88948181 intron variant T/C snv 0.49 5
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 5
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 5
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 4
rs7671167
FAM13A
0.925 0.040 4 88962828 intron variant C/T snv 0.53 4
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 4
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs546433642
KANSL1
0.925 0.120 17 46172742 intron variant T/C;G snv 4
rs549599956
KANSL1
0.925 0.120 17 46169798 intron variant A/G snv 4
rs12373139
MAPT-AS1 ; SPPL2C
0.925 0.120 17 45846764 missense variant G/A snv 0.15 0.14 4
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs199533
NSF ; LRRC37A2
0.925 0.120 17 46751565 synonymous variant G/A snv 0.13 0.13 4
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs1903003
FAM13A
0.925 0.080 4 88965146 intron variant C/G;T snv 3
rs2904259
FAM13A
4 88964563 intron variant T/A;C snv 3
rs2668692
KANSL1
1.000 0.040 17 46215654 intron variant G/A;T snv 3
rs7215239
LINC02210-CRHR1
1.000 0.040 17 45690407 intron variant T/C snv 0.30 3
rs2045517
LOC105377327 ; FAM13A
4 88949813 intron variant C/T snv 0.49 3
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 3
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