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rs796053092

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053092(C;G)
Make rs796053092(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166051944
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053092
ebirs796053092
HLIrs796053092
Exacrs796053092
Varsomers796053092
Maprs796053092
PheGenIrs796053092
hapmaprs796053092
1000 genomesrs796053092
hgdprs796053092
ensemblrs796053092
gopubmedrs796053092
geneviewrs796053092
scholarrs796053092
googlers796053092
pharmgkbrs796053092
gwascentralrs796053092
openSNPrs796053092
23andMers796053092
23andMe allrs796053092
SNP Nexus

SNPshotrs796053092
SNPdbers796053092
MSV3drs796053092
GWAS Ctlgrs796053092
Max Magnitude0
ClinVar
Risk rs796053092(G;G)
Alt rs796053092(G;G)
Reference rs796053092(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166908454G>C
CLNSRC
CLNACC RCV000189075.1,