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rs1064796343

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome2
Position165996032
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1064796343
dbSNP (classic)rs1064796343
ClinGenrs1064796343
ebirs1064796343
HLIrs1064796343
Exacrs1064796343
Gnomadrs1064796343
Varsomers1064796343
LitVarrs1064796343
Maprs1064796343
PheGenIrs1064796343
Biobankrs1064796343
1000 genomesrs1064796343
hgdprs1064796343
ensemblrs1064796343
geneviewrs1064796343
scholarrs1064796343
googlers1064796343
pharmgkbrs1064796343
gwascentralrs1064796343
openSNPrs1064796343
23andMers1064796343
SNPshotrs1064796343
SNPdbers1064796343
MSV3drs1064796343
GWAS Ctlgrs1064796343
Max Magnitude0
ClinVar
Risk rs1064796343(-;-)
Alt rs1064796343(-;-)
Reference Rs1064796343(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166852542delT
CLNSRC
CLNACC RCV000485464.1,