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rs797045942

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045942(A;A)
Make rs797045942(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165344559
GeneSCN2A
is asnp
is mentioned by
dbSNPrs797045942
ebirs797045942
HLIrs797045942
Exacrs797045942
Varsomers797045942
Maprs797045942
PheGenIrs797045942
hapmaprs797045942
1000 genomesrs797045942
hgdprs797045942
ensemblrs797045942
gopubmedrs797045942
geneviewrs797045942
scholarrs797045942
googlers797045942
pharmgkbrs797045942
gwascentralrs797045942
openSNPrs797045942
23andMers797045942
23andMe allrs797045942
SNP Nexus

SNPshotrs797045942
SNPdbers797045942
MSV3drs797045942
GWAS Ctlgrs797045942
Max Magnitude0
ClinVar
Risk rs797045942(A;A)
Alt rs797045942(A;A)
Reference rs797045942(G;G)
Significance Probable-Pathogenic
Disease Seizures
Variation info
Gene SCN2A
CLNDBN Seizures
Reversed 0
HGVS NC_000002.11:g.166201069G>A
CLNSRC
CLNACC RCV000193985.1,