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: rs121918733
rs121918733
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166058684 missense variant A/G snv 0.800 1.000 24 2003 2017
dbSNP: rs121918779
rs121918779
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165991933 missense variant T/C snv 0.700 1.000 24 2003 2017
dbSNP: rs121917922
rs121917922
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165992302 missense variant G/A;C snv 0.800 1.000 22 2003 2017
dbSNP: rs121917923
rs121917923
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166047725 missense variant G/A;T snv 0.800 1.000 22 2003 2017
dbSNP: rs121917938
rs121917938
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166051845 missense variant A/G snv 0.800 1.000 22 2003 2017
dbSNP: rs121917960
rs121917960
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 166002753 missense variant C/T snv 0.800 1.000 22 2003 2017
dbSNP: rs121917965
rs121917965
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166058652 missense variant G/A snv 0.800 1.000 22 2003 2017
dbSNP: rs121917980
rs121917980
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165991928 missense variant C/T snv 0.800 1.000 22 2003 2017
dbSNP: rs121917985
rs121917985
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166051968 missense variant C/T snv 0.800 1.000 22 2003 2017
dbSNP: rs121917990
rs121917990
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166043836 missense variant T/A;C snv 0.800 1.000 22 2003 2017
dbSNP: rs121918737
rs121918737
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166037868 missense variant A/C snv 0.800 1.000 22 2003 2017
dbSNP: rs121918738
rs121918738
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 166013820 missense variant G/A;T snv 1.6E-05 0.800 1.000 22 2003 2017
dbSNP: rs121918739
rs121918739
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 166012210 missense variant T/G snv 0.800 1.000 22 2003 2017
dbSNP: rs121918740
rs121918740
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 166012128 missense variant A/G snv 0.800 1.000 22 2003 2017
dbSNP: rs121918741
rs121918741
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165999763 missense variant C/T snv 0.800 1.000 22 2003 2017
dbSNP: rs121918742
rs121918742
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165994241 missense variant C/G;T snv 0.800 1.000 22 2003 2017
dbSNP: rs121918763
rs121918763
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165991929 missense variant G/A;C snv 2.8E-05 0.800 1.000 22 2003 2017
dbSNP: rs121918770
rs121918770
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166054710 missense variant C/A;T snv 0.800 1.000 22 2003 2017
dbSNP: rs121918773
rs121918773
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166054672 missense variant A/G snv 0.800 1.000 22 2003 2017
dbSNP: rs121917907
rs121917907
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166073435 missense variant A/G snv 7.0E-06 0.700 1.000 21 2003 2017
dbSNP: rs121917908
rs121917908
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165999764 stop gained C/A;G;T snv 0.700 1.000 21 2003 2017
dbSNP: rs121917909
rs121917909
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166051967 missense variant G/A snv 0.700 1.000 21 2003 2017
dbSNP: rs121917911
rs121917911
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 166013752 missense variant C/G snv 0.700 1.000 21 2003 2017
dbSNP: rs121917913
rs121917913
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 166002491 missense variant T/C snv 4.0E-06 0.700 1.000 21 2003 2017
dbSNP: rs121917914
rs121917914
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165992387 missense variant C/G;T snv 0.700 1.000 21 2003 2017