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rs796053091

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053091(C;C)
Make rs796053091(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166052875
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053091
ebirs796053091
HLIrs796053091
Exacrs796053091
Varsomers796053091
Maprs796053091
PheGenIrs796053091
hapmaprs796053091
1000 genomesrs796053091
hgdprs796053091
ensemblrs796053091
gopubmedrs796053091
geneviewrs796053091
scholarrs796053091
googlers796053091
pharmgkbrs796053091
gwascentralrs796053091
openSNPrs796053091
23andMers796053091
23andMe allrs796053091
SNP Nexus

SNPshotrs796053091
SNPdbers796053091
MSV3drs796053091
GWAS Ctlgrs796053091
Max Magnitude0
ClinVar
Risk rs796053091(C;C)
Alt rs796053091(C;C)
Reference rs796053091(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166909385A>G
CLNSRC
CLNACC RCV000189073.2,