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rs796053095

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053095(C;C)
Make rs796053095(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166041292
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053095
ebirs796053095
HLIrs796053095
Exacrs796053095
Varsomers796053095
Maprs796053095
PheGenIrs796053095
hapmaprs796053095
1000 genomesrs796053095
hgdprs796053095
ensemblrs796053095
gopubmedrs796053095
geneviewrs796053095
scholarrs796053095
googlers796053095
pharmgkbrs796053095
gwascentralrs796053095
openSNPrs796053095
23andMers796053095
23andMe allrs796053095
SNP Nexus

SNPshotrs796053095
SNPdbers796053095
MSV3drs796053095
GWAS Ctlgrs796053095
Max Magnitude0
ClinVar
Risk rs796053095(C;C)
Alt rs796053095(C;C)
Reference rs796053095(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166897802A>G
CLNSRC
CLNACC RCV000189083.1,