Source: ALL
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: rs1057516097
rs1057516097
KCNQ2
3 0.882 0.040 20 63439671 missense variant G/T snv 0.010 1.000 1 2019 2019
dbSNP: rs1060499553
rs1060499553
GABRA1
6 0.827 0.040 5 161890983 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs11615
rs11615
ERCC1
62 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 0.010 1.000 1 2017 2017
dbSNP: rs13181
rs13181
ERCC2 ; KLC3
134 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 0.010 < 0.001 1 2017 2017
dbSNP: rs1799793
rs1799793
ERCC2
72 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 0.010 1.000 1 2017 2017
dbSNP: rs324148
rs324148
SLC29A1
3 0.882 0.280 6 44228841 intron variant T/C snv 0.78 0.010 1.000 1 2014 2014
dbSNP: rs398122854
rs398122854
ARX
3 0.882 0.040 X 25015657 stop gained G/C snv 0.010 1.000 1 2010 2010
dbSNP: rs587777308
rs587777308
GABRA1
14 0.763 0.040 5 161873196 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs796052491
rs796052491
GABRA1
4 0.851 0.040 5 161890982 missense variant T/A;C snv 0.010 1.000 1 2016 2016
dbSNP: rs796052493
rs796052493
GABRA1
4 0.851 0.040 5 161895668 missense variant G/A;T snv 0.010 1.000 1 2016 2016