Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918364
SRPX2
0.851 0.200 X 100662227 missense variant A/C snv 3.3E-05 2.9E-05 5
rs672601376
LOC105369668 ; GRIN2B
0.925 0.040 12 13608760 missense variant A/C snv 3
rs1404008939
ABCB1
0.925 0.200 7 87504324 missense variant A/C;G snv 4.0E-06 4
rs225012
DIO2
1.000 0.200 14 80204392 intron variant A/C;G snv 0.51 2
rs16827801
PSMD1 ; HTR2B
2 231116063 intron variant A/C;G snv 0.40 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs267607048
SHOC2
0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 16
rs121918524
PHF8
0.827 0.200 X 54011232 missense variant A/G snv 6
rs104886492
HSD17B10
1.000 0.120 X 53432410 missense variant A/G snv 3
rs121917899
PQBP1
1.000 0.080 X 48901944 missense variant A/G snv 2
rs145390085
L2HGDH
1.000 0.040 14 50269297 missense variant A/G snv 2
rs749457448
DLG3 ; DLG3-AS1
1.000 0.200 X 70452622 start lost A/G snv 2
rs768560449
IMMT
1.000 0.160 2 86166521 missense variant A/G snv 8.1E-06 7.0E-06 2
rs864309721
CDC42
1.000 1 22086451 missense variant A/G snv 2
rs551253128
MID2 ; LOC101928335
X 107905581 missense variant A/G snv 1.3E-03 1.6E-04 1
rs132630328
GK
0.925 0.200 X 30720721 missense variant A/G;T snv 5.4E-06 3
rs968910165
NCAM2
21 21286370 missense variant A/G;T snv 4.0E-06 1.4E-05 1
rs121434613
PAK3
0.882 0.240 X 111194402 missense variant C/A snv 4
rs397514627
CAMK2G
0.882 0.160 10 73842486 missense variant C/A;G snv 5
rs5030849
PAH
0.851 0.280 12 102852875 missense variant C/A;G;T snv 2.2E-04 6
rs200115000
CAMK2B
1.000 0.160 7 44220165 missense variant C/A;G;T snv 2.6E-04; 5.8E-05 2
rs374073809
VASH2
1 212961166 missense variant C/A;G;T snv 4.0E-06; 1.6E-05; 3.2E-05 1
rs80338758
MED12
0.790 0.400 X 71127367 missense variant C/A;T snv 12
rs781908532
SLC25A1
0.827 0.160 22 19176585 missense variant C/A;T snv 4.0E-06; 1.6E-05 7.0E-06 8