Gene: SCN1A ×
Source: UNIPROT ×
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: rs121917918
rs121917918
SCN1A ; SCN1A-AS1
1 0.851 0.040 2 166058651 missense variant C/A;T snv 0.800 1.000 24 2003 2017
dbSNP: rs121917927
rs121917927
SCN1A ; SCN1A-AS1
1 0.925 0.040 2 166046969 missense variant C/G;T snv 0.800 1.000 24 2003 2017
dbSNP: rs121918733
rs121918733
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166058684 missense variant A/G snv 0.800 1.000 23 2003 2017
dbSNP: rs121917921
rs121917921
SCN1A ; SCN1A-AS1 ; LOC102724058
1 0.882 0.040 2 165991927 missense variant G/A snv 0.800 1.000 21 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 21 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 21 2003 2017
dbSNP: rs121917929
rs121917929
SCN1A ; SCN1A-AS1
1 0.925 0.160 2 166046970 missense variant G/A;T snv 0.800 1.000 21 2003 2017
dbSNP: rs121917935
rs121917935
SCN1A ; SCN1A-AS1
1 0.851 0.040 2 166054660 missense variant C/A;T snv 0.800 1.000 21 2003 2017
dbSNP: rs121917937
rs121917937
SCN1A ; SCN1A-AS1
1 0.925 0.040 2 166052866 missense variant A/C snv 0.800 1.000 21 2003 2017
dbSNP: rs121917938
rs121917938
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166051845 missense variant A/G snv 0.800 1.000 21 2003 2017
dbSNP: rs121917959
rs121917959
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166058599 missense variant C/A;G;T snv 4.0E-06 0.800 1.000 21 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 21 2003 2017
dbSNP: rs121917964
rs121917964
SCN1A ; SCN1A-AS1
1 0.851 0.080 2 166073371 missense variant T/C snv 0.800 1.000 21 2003 2017
dbSNP: rs121917965
rs121917965
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166058652 missense variant G/A snv 0.800 1.000 21 2003 2017
dbSNP: rs121917971
rs121917971
SCN1A ; SCN1A-AS1
2 0.851 0.080 2 166037885 missense variant C/G;T snv 0.800 1.000 21 2003 2017
dbSNP: rs121917976
rs121917976
SCN1A ; SCN1A-AS1 ; LOC102724058
1 0.882 0.080 2 165992341 missense variant C/G;T snv 0.800 1.000 21 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 21 2003 2017
dbSNP: rs121917984
rs121917984
SCN1A ; SCN1A-AS1
1 0.790 0.080 2 166052869 missense variant G/A;C snv 0.800 1.000 21 2003 2017
dbSNP: rs121917985
rs121917985
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166051968 missense variant C/T snv 0.800 1.000 21 2003 2017
dbSNP: rs121917986
rs121917986
SCN1A ; SCN1A-AS1 ; LOC102724058
1 0.882 0.040 2 166002588 missense variant C/G;T snv 0.800 1.000 21 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 21 2003 2017
dbSNP: rs121918625
rs121918625
SCN1A ; SCN1A-AS1 ; LOC102724058
1 0.925 0.040 2 166036521 missense variant G/A snv 0.800 1.000 21 2003 2017
dbSNP: rs121918735
rs121918735
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166051906 missense variant G/A;T snv 3.2E-05 0.800 1.000 21 2003 2017
dbSNP: rs121918736
rs121918736
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166037907 missense variant G/A;C snv 0.800 1.000 21 2003 2017
dbSNP: rs121918737
rs121918737
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166037868 missense variant A/C snv 0.800 1.000 21 2003 2017