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rs587780446

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780446(-;-)
Make rs587780446(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position165991478
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs587780446
ebirs587780446
HLIrs587780446
Exacrs587780446
Varsomers587780446
Maprs587780446
PheGenIrs587780446
hapmaprs587780446
1000 genomesrs587780446
hgdprs587780446
ensemblrs587780446
gopubmedrs587780446
geneviewrs587780446
scholarrs587780446
googlers587780446
pharmgkbrs587780446
gwascentralrs587780446
openSNPrs587780446
23andMers587780446
23andMe allrs587780446
SNP Nexus

SNPshotrs587780446
SNPdbers587780446
MSV3drs587780446
GWAS Ctlgrs587780446
Max Magnitude0
ClinVar
Risk rs587780446(;)
Alt rs587780446(;)
Reference rs587780446(C;C)
Significance Pathogenic
Disease Generalized epilepsy with febrile seizures plus
Variation info
Gene LOC102724058 SCN1A
CLNDBN Generalized epilepsy with febrile seizures plus, type 2
Reversed 1
HGVS NC_000002.11:g.166847988delG
CLNSRC
CLNACC RCV000118238.1,