Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918626
LOC102724058 ; SCN1A ; SCN1A-AS1
0.925 0.080 2 166012179 missense variant T/G snv 3
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs12765063
CUL2 ; CREM
10 35127641 intron variant G/A snv 0.14 2
rs1331851285
CASP1
1.000 0.080 11 105029220 missense variant T/C snv 1.4E-05 2
rs1334791875
APP
21 25982369 missense variant G/A snv 4.0E-06 1
rs1365502141
APP
21 26000017 missense variant G/A snv 7.0E-06 1
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv 10
rs148881970
NAGLU
0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22
rs150450891
FTO
16 53826341 missense variant G/A snv 4.6E-04 5.7E-04 1
rs1541665
KCNIP1
1.000 0.040 5 170715913 intron variant C/G;T snv 0.21 2
rs1553920379
PPP3CA
0.776 0.160 4 101032294 frameshift variant -/AGTA delins 27
rs1555582065
UBTF ; LOC101926967
0.827 0.160 17 44212851 missense variant C/T snv 13
rs1566785444
IRF2BPL
0.827 0.200 14 77025671 frameshift variant C/- delins 20
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs1800035
ADRA2A
0.925 0.080 10 111078794 missense variant C/G;T snv 1.9E-03 4
rs1800544
ADRA2A
0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 12
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs202064075
CLCNKB
1 16048352 missense variant G/A snv 1.5E-04 7.7E-05 1
rs202151337
SCN8A
0.925 0.160 12 51806788 missense variant A/G snv 4
rs202247812
KRAS
1.000 0.160 12 25225717 missense variant T/C snv 2
rs206936
RPS10-NUDT3 ; NUDT3
0.882 0.160 6 34335092 intron variant A/G snv 0.34 8
rs2110267
DPP6
1.000 0.040 7 153838604 intergenic variant C/G snv 0.32 3
rs2161961
GNAL
18 11774501 intron variant A/G snv 0.31 3
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52