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: rs121917940
rs121917940
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166046871 missense variant A/T snv 0.700 1.000 21 2003 2017
dbSNP: rs121917941
rs121917941
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166039577 stop gained G/C snv 0.700 1.000 21 2003 2017
dbSNP: rs121917942
rs121917942
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166039476 stop gained C/A;T snv 0.700 1.000 21 2003 2017
dbSNP: rs121917943
rs121917943
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166037897 missense variant A/G snv 0.700 1.000 21 2003 2017
dbSNP: rs121917944
rs121917944
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 166002479 missense variant A/C snv 0.700 1.000 21 2003 2017
dbSNP: rs121917946
rs121917946
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165998126 missense variant A/G snv 0.700 1.000 21 2003 2017
dbSNP: rs121917947
rs121917947
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165998090 missense variant A/G snv 0.700 1.000 21 2003 2017
dbSNP: rs121917948
rs121917948
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165992273 missense variant G/C snv 0.700 1.000 21 2003 2017
dbSNP: rs121917949
rs121917949
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165992134 missense variant A/C;G snv 0.700 1.000 21 2003 2017
dbSNP: rs121917950
rs121917950
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165991990 missense variant C/T snv 0.700 1.000 21 2003 2017
dbSNP: rs121917952
rs121917952
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165991936 missense variant A/G snv 0.700 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: rs121917961
rs121917961
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 166002683 missense variant C/G snv 0.700 1.000 21 2003 2017
dbSNP: rs121917962
rs121917962
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165998129 missense variant T/C snv 0.700 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: rs121917966
rs121917966
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166046940 missense variant A/G snv 0.700 1.000 21 2003 2017
dbSNP: rs121917967
rs121917967
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166046910 missense variant A/T snv 0.700 1.000 21 2003 2017
dbSNP: rs121917968
rs121917968
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166041298 missense variant A/G snv 0.700 1.000 21 2003 2017
dbSNP: rs121917970
rs121917970
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166037889 missense variant A/G snv 0.700 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: rs121917974
rs121917974
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165999740 missense variant C/G;T snv 0.700 1.000 21 2003 2017
dbSNP: rs121917975
rs121917975
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165994365 missense variant T/C snv 0.700 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: rs121917977
rs121917977
SCN1A ; SCN1A-AS1 ; LOC102724058
1 1.000 0.040 2 165992156 missense variant A/C snv 0.700 1.000 21 2003 2017