Source: BEFREE ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs387906684
rs387906684
SCN2A
2 0.851 0.120 2 165367327 stop gained G/A;T snv 0.020 1.000 2 2009 2015
dbSNP: rs1045642
rs1045642
ABCB1
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2011 2011
dbSNP: rs10482672
rs10482672
NR3C1
2 0.925 0.080 5 143312968 intron variant G/A snv 0.15 0.010 1.000 1 2012 2012
dbSNP: rs11872992
rs11872992
MC4R
4 0.851 0.160 18 60373354 intron variant G/A snv 0.12 0.010 1.000 1 2007 2007
dbSNP: rs13397210
rs13397210
SCN1A ; SCN1A-AS1
2 0.925 0.080 2 166065518 intron variant C/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs242948
rs242948
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
2 0.925 0.080 17 45836178 intron variant G/C;T snv 0.010 < 0.001 1 2015 2015
dbSNP: rs267608472
rs267608472
CDKL5
2 0.882 0.160 X 18579965 stop gained C/T snv 0.010 1.000 1 2012 2012
dbSNP: rs267608493
rs267608493
CDKL5
2 0.827 0.200 X 18584331 missense variant C/A;T snv 0.010 1.000 1 2012 2012
dbSNP: rs2963155
rs2963155
NR3C1
3 0.882 0.160 5 143376439 intron variant A/G snv 0.24 0.010 1.000 1 2012 2012
dbSNP: rs370114048
rs370114048
SCN2A
3 0.882 0.080 2 165310541 missense variant A/G;T snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs398122394
rs398122394
ALG13
2 0.763 0.240 X 111685040 missense variant A/G snv 0.010 1.000 1 2016 2016
dbSNP: rs4912905
rs4912905
NR3C1
3 0.925 0.080 5 143350811 intron variant G/C snv 0.20 0.010 1.000 1 2012 2012
dbSNP: rs6877893
rs6877893
NR3C1
2 0.925 0.080 5 143347628 intron variant G/A snv 0.52 0.010 1.000 1 2012 2012
dbSNP: rs74315390
rs74315390
KCNQ2
6 0.790 0.120 20 63439609 missense variant C/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs760543
rs760543
LARGE1
2 0.925 0.080 22 33435602 intron variant C/T snv 0.38 0.010 1.000 1 2014 2014
dbSNP: rs796052621
rs796052621
KCNQ2
4 0.827 0.080 20 63444756 missense variant C/T snv 0.010 1.000 1 2017 2017
dbSNP: rs796053134
rs796053134
SCN2A
4 0.827 0.080 2 165374737 missense variant T/C snv 0.010 1.000 1 2016 2016