Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs864622194
RAB9B ; PLP1
0.925 0.080 X 103776997 start lost T/C;G snv 3
rs180177035
BRAF
0.752 0.280 7 140801502 missense variant T/C snv 35
rs1135402761
SYT1
0.827 0.320 12 79448958 missense variant T/C snv 11
rs869312825
GNB1
0.827 0.120 1 1804548 start lost T/C snv 11
rs869312823
GNB1
0.882 0.080 1 1806509 missense variant T/C snv 9
rs141970897
CRAT
0.925 0.200 9 129104269 missense variant T/C snv 1.1E-03 7.8E-04 8
rs869312821
GNB1
0.882 0.120 1 1806515 missense variant T/C snv 7
rs767982852
RUBCN
0.882 0.080 3 197694417 missense variant T/C snv 8.0E-06 4.9E-05 6
rs1114167298
GRM7
0.882 0.120 3 6861849 missense variant T/C snv 7.0E-06 5
rs148234606
SLC52A2
0.925 8 144360604 missense variant T/C snv 7.0E-05 7.7E-05 4
rs754320812
FBXL6 ; SLC52A2
0.925 8 144360427 missense variant T/C snv 2.4E-05 3.5E-05 4
rs1468358104
FLVCR1 ; FLVCR1-DT
1 212858454 start lost T/C snv 3.7E-05 3
rs797044860
CREBBP
0.925 0.120 16 3736801 missense variant T/C snv 3
rs121918329
HIBCH
1.000 0.080 2 190290425 missense variant T/C snv 6.4E-05 1.4E-05 2
rs1553194162
GNB1
1.000 1 1804496 missense variant T/C snv 2
rs1554100923
GABRG2
5 162149212 missense variant T/C snv 2
rs1554129113
PURA
5 140114873 missense variant T/C snv 2
rs1555247469
MED13L
1.000 12 116006413 splice acceptor variant T/C snv 2
rs1555408829
DYNC1H1
1.000 14 101994794 missense variant T/C snv 2
rs1555943503
RPS6KA3
1.000 X 20195156 intron variant T/C snv 2
rs793888527
PURA
1.000 5 140114744 missense variant T/C snv 2
rs1553689580
SLC6A1
3 11025543 missense variant T/C snv 1
rs1553881788
SEPSECS
4 25156889 missense variant T/C snv 1
rs1557045066
SLC6A8
X 153693368 splice donor variant T/C snv 1
rs797044897
ATP1A3
19 41984940 missense variant T/C snv 1