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rs796053097

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053097(C;C)
Make rs796053097(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166073440
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053097
ebirs796053097
HLIrs796053097
Exacrs796053097
Varsomers796053097
Maprs796053097
PheGenIrs796053097
hapmaprs796053097
1000 genomesrs796053097
hgdprs796053097
ensemblrs796053097
gopubmedrs796053097
geneviewrs796053097
scholarrs796053097
googlers796053097
pharmgkbrs796053097
gwascentralrs796053097
openSNPrs796053097
23andMers796053097
23andMe allrs796053097
SNP Nexus

SNPshotrs796053097
SNPdbers796053097
MSV3drs796053097
GWAS Ctlgrs796053097
Max Magnitude0
ClinVar
Risk rs796053097(C;C)
Alt rs796053097(C;C)
Reference rs796053097(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166929950A>G
CLNSRC
CLNACC RCV000189088.1,