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rs387906684

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906684(A;A)
Make rs387906684(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position165367327
GeneSCN2A
is asnp
is mentioned by
dbSNPrs387906684
ebirs387906684
HLIrs387906684
Exacrs387906684
Varsomers387906684
Maprs387906684
PheGenIrs387906684
hapmaprs387906684
1000 genomesrs387906684
hgdprs387906684
ensemblrs387906684
gopubmedrs387906684
geneviewrs387906684
scholarrs387906684
googlers387906684
pharmgkbrs387906684
gwascentralrs387906684
openSNPrs387906684
23andMers387906684
23andMe allrs387906684
SNP Nexus

SNPshotrs387906684
SNPdbers387906684
MSV3drs387906684
GWAS Ctlgrs387906684
Max Magnitude0
ClinVar
Risk rs387906684(A;A)
Alt rs387906684(A;A)
Reference rs387906684(G;G)
Significance Other
Disease Early infantile epileptic encephalopathy 11 Benign familial neonatal-infantile seizures not provided
Variation info
Gene SCN2A
CLNDBN Early infantile epileptic encephalopathy 11 Benign familial neonatal-infantile seizures not provided
Reversed 0
HGVS NC_000002.11:g.166223837G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022767.23, RCV000118248.1, RCV000189138.2,