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rs796052984

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052984(C;C)
Make rs796052984(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166038000
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052984
ebirs796052984
HLIrs796052984
Exacrs796052984
Varsomers796052984
Maprs796052984
PheGenIrs796052984
hapmaprs796052984
1000 genomesrs796052984
hgdprs796052984
ensemblrs796052984
gopubmedrs796052984
geneviewrs796052984
scholarrs796052984
googlers796052984
pharmgkbrs796052984
gwascentralrs796052984
openSNPrs796052984
23andMers796052984
23andMe allrs796052984
SNP Nexus

SNPshotrs796052984
SNPdbers796052984
MSV3drs796052984
GWAS Ctlgrs796052984
Max Magnitude0
ClinVar
Risk rs796052984(C;C)
Alt rs796052984(C;C)
Reference rs796052984(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894510C>G
CLNSRC
CLNACC RCV000188895.1,