Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9925477
SEC14L5
16 4973060 intron variant T/G snv 0.40 1
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs9900280
TAOK1
17 29442580 intron variant G/A snv 0.58 1
rs9891920
TAOK1
17 29446271 intron variant A/G;T snv 1
rs987044
SSH1
12 108856580 intron variant A/C;G snv 1
rs972578
PACSIN2
22 42991689 intron variant G/T snv 0.60 1
rs9660992
TMCC2
1 205280322 intron variant A/G snv 0.43 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9616907 22 50668551 upstream gene variant G/A;C snv 1
rs9573569
TBC1D4
13 75484835 upstream gene variant T/C snv 0.32 1
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 11
rs9473147 6 47641856 regulatory region variant A/G snv 0.27 2
rs944002
EXOC3L4
14 103106478 intron variant A/G snv 0.25 3
rs9402686
LOC105378010
6 135106679 upstream gene variant G/A snv 0.20 5
rs939563
INPP5K
17 1512616 intron variant T/A snv 0.50 1
rs9393294
LOC105374971 ; CASC15
6 22465392 intron variant C/T snv 0.13 1
rs9378796
SLC22A23
6 3448411 intron variant G/T snv 0.27 1
rs9378249 0.925 0.160 6 31359924 upstream gene variant T/A;G snv 3
rs896322
LOC101929459 ; TMCC2
1 205240617 intron variant A/G snv 0.92 1
rs893001
CD226
18 69849610 intron variant A/C snv 0.18 1
rs8109288
TPM4
19 16074749 non coding transcript exon variant G/A snv 3.9E-02 2
rs8106212
VAV1
19 6802560 intron variant C/T snv 3.2E-02 2
rs8076739 17 29387569 intron variant C/T snv 0.64 1
rs80226907 14 55198171 intron variant A/C snv 5.8E-02 1
rs8022206
RAD51B
14 68054189 intron variant G/A snv 0.18 2