Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9331888
CLU ; MIR6843
0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 1
rs9304861 1.000 0.080 19 34780984 upstream gene variant A/G snv 0.13 1
rs9304644
APOC2 ; APOC4-APOC2
1.000 0.080 19 44946776 intron variant C/G;T snv 1
rs9302457
CLEC16A
1.000 0.080 16 10965980 intron variant G/A snv 0.43 1
rs9293513
MEF2C-AS1
1.000 0.080 5 89337967 intron variant G/A snv 3.0E-02 1
rs9271192 1.000 0.080 6 32610753 intergenic variant C/A snv 0.74 1
rs9269853
HLA-DRB1
1.000 0.080 6 32582545 intron variant A/C;T snv 1
rs9268877
HLA-DRB9
0.827 0.200 6 32463370 intron variant A/G;T snv 4
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 4
rs917570
RPS6KB2
1.000 0.080 11 67429073 non coding transcript exon variant C/G;T snv 0.30; 2.2E-02 1
rs913361
PALM2AKAP2
1.000 0.080 9 109849245 intron variant G/A snv 0.14 1
rs913360
PALM2AKAP2
1.000 0.080 9 109849099 intron variant T/G snv 0.16 1
rs912322
LOC105370356 ; MYO16
1.000 0.080 13 109155938 intron variant A/G snv 0.23 1
rs906454643
PSEN1
0.882 0.080 14 73217219 missense variant T/C snv 4.0E-06 1
rs901104
GAB2 ; USP35
1.000 0.080 11 78219453 intron variant G/A snv 0.22 0.15 1
rs889555
BCKDK
1.000 0.080 16 31111250 intron variant C/T snv 0.34 0.33 1
rs886041116
ADNP
0.776 0.240 20 50892526 stop gained G/A snv 11
rs879255085
LDLR
0.925 0.160 19 11120203 missense variant G/A;T snv 1
rs867611
PICALM
1.000 0.080 11 86065502 intron variant G/A snv 0.73 1
rs866500
CASTOR3
1.000 0.080 7 100242838 intron variant A/G;T snv 1
rs866101707
VCP
1.000 0.080 9 35066711 missense variant G/A snv 1
rs858502
CASTOR3
1.000 0.080 7 100245730 intron variant T/C snv 0.50 1
rs857551
LOC107987301
1.000 0.080 21 43410112 downstream gene variant A/C snv 0.13 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs854384 1.000 0.080 14 24802314 regulatory region variant T/A;C snv 1