Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9930139
RBFOX1
1.000 0.040 16 7239569 intron variant A/C;T snv 2
rs9904290
LOC105371800 ; MAPT
1.000 0.040 17 45924905 intron variant A/G snv 0.53 2
rs9858071
PLCL2
1.000 0.040 3 16803898 intron variant T/C snv 0.37 2
rs9852417
LINC02040 ; LOC105377127
1.000 0.040 3 65175479 intron variant C/A snv 0.66 2
rs9586
KLHDC8B
1.000 0.040 3 49176204 3 prime UTR variant C/G;T snv 2
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 5
rs913687
RABGAP1L
1.000 0.040 1 174805993 intron variant A/G snv 0.60 2
rs896686
TCF4-AS1 ; TCF4
1.000 0.040 18 55455800 intron variant T/G snv 0.12 2
rs841
GCH1
0.827 0.200 14 54843774 splice region variant G/A snv 0.22 0.22 1
rs836927 1.000 0.040 3 107482581 intergenic variant C/A snv 0.52 2
rs8100891 1.000 0.040 19 32338607 intergenic variant C/A;G snv 3
rs8097041
DCC
1.000 0.040 18 53371847 intron variant A/T snv 0.55 2
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs8067056
MAPT
0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs80278479
TFAP2D
0.925 0.040 6 50758466 intron variant C/G snv 3.0E-03 3
rs80164876
LOC105374732 ; EGFLAM
1.000 0.040 5 38464142 3 prime UTR variant A/G snv 1.9E-02 3
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 1
rs8004430
AREL1
1.000 0.040 14 74704980 intron variant C/T snv 0.72 2
rs80035064
CELF4
1.000 0.040 18 37566403 intron variant T/A snv 0.18 2
rs7939345 1.000 0.040 11 47959016 intergenic variant T/A;G snv 3
rs7937477 1.000 0.040 11 113545374 intergenic variant A/T snv 0.59 2
rs7927724
CREB3L1
1.000 0.040 11 46301658 intron variant G/A snv 0.32 2
rs7927693 1.000 0.040 11 113554746 intergenic variant G/A snv 0.57 2
rs7912226 1.000 0.040 10 105892386 intron variant T/A snv 0.44 2
rs7827176 1.000 0.040 8 91637324 intron variant A/T snv 0.55 2