Source: INFERRED ×
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 1
rs672601376
LOC105369668 ; GRIN2B
0.925 0.040 12 13608760 missense variant A/C snv 1
rs267607048
SHOC2
0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 12
rs121917899
PQBP1
1.000 0.080 X 48901944 missense variant A/G snv 1
rs121918524
PHF8
0.827 0.200 X 54011232 missense variant A/G snv 1
rs864309721
CDC42
1.000 1 22086451 missense variant A/G snv 1
rs132630328
GK
0.925 0.200 X 30720721 missense variant A/G;T snv 5.4E-06 1
rs121434613
PAK3
0.882 0.240 X 111194402 missense variant C/A snv 1
rs397514627
CAMK2G
0.882 0.160 10 73842486 missense variant C/A;G snv 4
rs5030849
PAH
0.851 0.280 12 102852875 missense variant C/A;G;T snv 2.2E-04 1
rs80338758
MED12
0.790 0.400 X 71127367 missense variant C/A;T snv 9
rs781908532
SLC25A1
0.827 0.160 22 19176585 missense variant C/A;T snv 4.0E-06; 1.6E-05 7.0E-06 5
rs45517305
TSC2
0.851 0.240 16 2081646 stop gained C/A;T snv 1
rs113994097
POLG
0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 5
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 1
rs61750420
PEX1
0.689 0.480 7 92501562 missense variant C/T snv 3.2E-04 3.5E-04 46
rs398123009
PACS1
0.790 0.200 11 66211206 missense variant C/T snv 7.0E-06 17
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs387907281
ATP1A3
0.752 0.280 19 41970284 missense variant C/T snv 6
rs121965020
SLC26A1 ; IDUA
0.827 0.280 4 987858 stop gained C/T snv 4.7E-04 6.1E-04 4
rs1057516085
KCNQ2
0.827 0.080 20 63444747 missense variant C/T snv 2
rs863225264
MTOR
0.827 0.240 1 11130747 missense variant C/T snv 2
rs886041761
KCNA2
0.925 0.200 1 110603902 missense variant C/T snv 2
rs1057519087
MFSD2A
0.925 0.120 1 39967632 missense variant C/T snv 7.0E-06 1
rs1131692042
RPL10 ; SNORA70
0.925 0.120 X 154399803 missense variant C/T snv 1