Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 10
rs165656
COMT
0.925 0.200 22 19961340 intron variant G/A;C;T snv 5
rs723744
TTR
0.925 0.200 18 31592513 intron variant G/T snv 0.38 3
rs752306
DRD4
0.925 0.200 11 637622 intron variant C/T snv 6.4E-02 4.8E-02 3
rs225010
DIO2
1.000 0.200 14 80205936 intron variant C/T snv 0.51 2
rs225012
DIO2
1.000 0.200 14 80204392 intron variant A/C;G snv 0.51 2
rs6511901
CC2D1A
1.000 0.200 19 13916839 intron variant C/T snv 0.39 2
rs6530893
TUSC3
1.000 0.200 8 15671068 intron variant T/C snv 0.14 2
rs6994908
TUSC3
1.000 0.200 8 15674943 intron variant T/C snv 0.32 2
rs10194776
PSMD1 ; HTR2B
2 231115305 intron variant C/T snv 0.54 1
rs16827801
PSMD1 ; HTR2B
2 231116063 intron variant A/C;G snv 0.40 1
rs255012 1.000 0.200 7 41189487 regulatory region variant T/A;C snv 2
rs879255652
SCN8A
0.807 0.120 12 51790425 stop gained G/A;T snv 7
rs121965020
SLC26A1 ; IDUA
0.827 0.280 4 987858 stop gained C/T snv 4.7E-04 6.1E-04 6
rs45517305
TSC2
0.851 0.240 16 2081646 stop gained C/A;T snv 5
rs121918368
CRBN ; TRNT1
0.925 0.200 3 3150939 stop gained G/A snv 8.0E-06 7.0E-06 3
rs121918523
PHF8
0.925 0.200 X 54016662 stop gained T/A snv 3
rs122468181
UPF3B
0.925 0.200 X 119837771 stop gained G/A;T snv 3
rs61751367
MECP2
0.925 0.080 X 154030939 stop gained G/A snv 3
rs1427146168
NUP214
1.000 0.200 9 131140671 stop gained C/T snv 2
rs1464216639
MAN1B1
1.000 9 137106289 stop gained G/A snv 6.1E-06 2
rs281860639
MIR6894 ; KDM5C
1.000 0.080 X 53199048 stop gained G/T snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272