Gene: SCN1A ×
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: rs121917927
rs121917927
SCN1A ; SCN1A-AS1
2 0.925 0.040 2 166046969 missense variant C/G;T snv 0.800 1.000 32 2003 2017
dbSNP: rs121917971
rs121917971
SCN1A ; SCN1A-AS1
4 0.851 0.080 2 166037885 missense variant C/G;T snv 0.800 1.000 31 2003 2017
dbSNP: rs121917918
rs121917918
SCN1A ; SCN1A-AS1
4 0.851 0.040 2 166058651 missense variant C/A;T snv 0.800 1.000 25 2003 2017
dbSNP: rs121918775
rs121918775
SCN1A ; SCN1A-AS1
5 0.827 0.080 2 166037886 missense variant G/A;T snv 0.800 1.000 25 2003 2017
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: rs121917969
rs121917969
SCN1A ; SCN1A-AS1
2 0.925 0.040 2 166037891 missense variant A/G snv 0.700 1.000 23 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: rs121917937
rs121917937
SCN1A ; SCN1A-AS1
2 0.925 0.040 2 166052866 missense variant A/C 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: 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: 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: rs121918735
rs121918735
SCN1A ; SCN1A-AS1
2 1.000 0.040 2 166051906 missense variant G/A;T snv 3.2E-05 0.800 1.000 22 2003 2017
dbSNP: rs121918736
rs121918736
SCN1A ; SCN1A-AS1
2 1.000 0.040 2 166037907 missense variant G/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: 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: 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: rs121917917
rs121917917
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166037852 missense variant C/A snv 0.700 1.000 21 2003 2017
dbSNP: rs121917920
rs121917920
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166047731 missense variant T/C snv 0.700 1.000 21 2003 2017
dbSNP: rs121917929
rs121917929
SCN1A ; SCN1A-AS1
3 0.925 0.160 2 166046970 missense variant G/A;T snv 0.800 1.000 21 2003 2017
dbSNP: rs121917933
rs121917933
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166073388 missense variant C/A;T snv 8.0E-06 0.700 1.000 21 2003 2017
dbSNP: rs121917934
rs121917934
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166054756 missense variant T/G snv 0.700 1.000 21 2003 2017
dbSNP: rs121917935
rs121917935
SCN1A ; SCN1A-AS1
4 0.851 0.040 2 166054660 missense variant C/A;T snv 0.800 1.000 21 2003 2017