Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912562
NR3C2
0.925 0.160 4 148435252 stop gained G/A;C snv 4.0E-06 2
rs1553518509
MBD5
1.000 0.040 2 148468916 stop gained C/T snv 2
rs886037776
EHMT1
0.925 0.280 9 137817477 stop gained G/A snv 2
rs1569513495
SBF1
1.000 0.040 22 50465238 stop gained C/A snv 1
rs397514679
SYN1
0.790 0.200 X 47574321 stop gained G/A snv 1
rs796052733
MEF2C
1.000 0.040 5 88731773 stop gained G/A snv 1
rs28934908
MECP2
0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 12
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs863225082
PPP2R5D ; MEA1
0.827 0.160 6 43007265 missense variant G/A snv 7
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs727504317
MAP2K1
0.807 0.320 15 66435145 missense variant G/A snv 6
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs797045050
KIF1A
0.807 0.120 2 240797715 missense variant C/T snv 4
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs121917893
NLGN3
0.807 0.160 X 71167508 missense variant C/T snv 2
rs121918799
SCN1A-AS1 ; SCN1A ; LOC102724058
0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 2
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 2
rs1131692040
SNORA70 ; RPL10
0.882 0.160 X 154399844 missense variant A/G snv 1
rs121908445
CNTNAP2
0.925 0.040 7 148147542 missense variant T/C snv 3.3E-04 1.7E-04 1
rs1276388879
POGZ
1.000 0.040 1 151405647 missense variant A/C;G snv 1
rs1372713010
POGZ
1.000 0.040 1 151428041 missense variant G/A snv 1
rs1418634444
POGZ
1.000 0.040 1 151408777 missense variant T/C snv 7.0E-06 1
rs1452048149
POGZ
1.000 0.040 1 151404828 missense variant C/T snv 4.0E-06 1
rs1476293577
POGZ
1.000 0.040 1 151428188 missense variant G/A;C snv 1
rs1484207450
POGZ
1.000 0.040 1 151405155 missense variant A/G snv 7.0E-06 1