Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11450220
MAFF ; PLA2G6
22 38211527 intron variant -/G delins 0.58 1
rs118173451
TTC28-AS1
22 27960612 intron variant T/C snv 1.1E-02 1
rs12170305
ZC3H7B
22 41346279 intron variant G/A snv 3.6E-02 1
rs13057352
CERK
22 46699338 missense variant C/A snv 2.6E-02 2.6E-02 1
rs134077 22 27667264 intergenic variant G/A snv 0.39 1
rs136029
ATXN10
22 45840545 intron variant G/A snv 0.46 1
rs136139
TBC1D22A
22 46992426 intron variant G/A;C snv 0.31 1
rs136872
DEPDC5
22 31885582 intron variant A/G snv 0.94 1
rs139030
SCUBE1
22 43257619 intron variant A/G snv 0.20 1
rs139420 22 39161409 intergenic variant C/T snv 0.16 1
rs145952310
ZNF70
22 23744998 missense variant T/C snv 1.8E-03 7.0E-04 1
rs2294358
MYH9
22 36375211 intron variant G/C snv 4.1E-02 1
rs2413143
LOC105373002 ; SYN3
22 32660873 intron variant C/T snv 0.26 1
rs28567375 22 46021443 intergenic variant C/A snv 9.7E-02 1
rs433704
LOC107985532
22 21660633 intron variant C/A;G;T snv 1
rs4373007
SYN3 ; LOC105373002
22 32650550 intron variant C/G snv 0.20 1
rs55906059
MEI1
22 41788139 intron variant C/T snv 7.0E-02 1
rs5750691
LOC105373032
22 38885769 upstream gene variant T/G snv 0.18 1
rs5753566
PATZ1
22 31339226 intron variant A/G snv 4.0E-02 1
rs5754283
SYN3
22 32781404 intron variant T/G snv 0.26 1
rs5758999
PACSIN2
22 42866734 intron variant T/C snv 0.43 1
rs5766632 22 45300814 downstream gene variant G/A;C snv 1
rs58280444
MIRLET7BHG
22 46088037 intron variant G/A snv 3.4E-02 1
rs6000890 22 37791294 regulatory region variant C/T snv 0.66 1
rs7284660
CYB5R3 ; ATP5MGL
22 42640773 intron variant G/A;C snv 1