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rs796053006

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053006(C;C)
Make rs796053006(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166002729
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053006
ebirs796053006
HLIrs796053006
Exacrs796053006
Varsomers796053006
Maprs796053006
PheGenIrs796053006
hapmaprs796053006
1000 genomesrs796053006
hgdprs796053006
ensemblrs796053006
gopubmedrs796053006
geneviewrs796053006
scholarrs796053006
googlers796053006
pharmgkbrs796053006
gwascentralrs796053006
openSNPrs796053006
23andMers796053006
23andMe allrs796053006
SNP Nexus

SNPshotrs796053006
SNPdbers796053006
MSV3drs796053006
GWAS Ctlgrs796053006
Max Magnitude0
ClinVar
Risk rs796053006(C;C)
Alt rs796053006(C;C)
Reference rs796053006(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166859239C>G
CLNSRC
CLNACC RCV000188941.2,