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rs796052977

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052977(A;A)
Make rs796052977(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166045043
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052977
ebirs796052977
HLIrs796052977
Exacrs796052977
Varsomers796052977
Maprs796052977
PheGenIrs796052977
hapmaprs796052977
1000 genomesrs796052977
hgdprs796052977
ensemblrs796052977
gopubmedrs796052977
geneviewrs796052977
scholarrs796052977
googlers796052977
pharmgkbrs796052977
gwascentralrs796052977
openSNPrs796052977
23andMers796052977
23andMe allrs796052977
SNP Nexus

SNPshotrs796052977
SNPdbers796052977
MSV3drs796052977
GWAS Ctlgrs796052977
Max Magnitude0
ClinVar
Risk rs796052977(A;A)
Alt rs796052977(A;A)
Reference rs796052977(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166901553C>T
CLNSRC
CLNACC RCV000188875.2,