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rs796053094

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053094(C;C)
Make rs796053094(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166046943
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053094
ebirs796053094
HLIrs796053094
Exacrs796053094
Varsomers796053094
Maprs796053094
PheGenIrs796053094
hapmaprs796053094
1000 genomesrs796053094
hgdprs796053094
ensemblrs796053094
gopubmedrs796053094
geneviewrs796053094
scholarrs796053094
googlers796053094
pharmgkbrs796053094
gwascentralrs796053094
openSNPrs796053094
23andMers796053094
23andMe allrs796053094
SNP Nexus

SNPshotrs796053094
SNPdbers796053094
MSV3drs796053094
GWAS Ctlgrs796053094
Max Magnitude0
ClinVar
Risk rs796053094(C;C)
Alt rs796053094(C;C)
Reference rs796053094(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166903453A>G
CLNSRC
CLNACC RCV000189079.2,