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rs796052970

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052970(C;C)
Make rs796052970(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166047703
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052970
ebirs796052970
HLIrs796052970
Exacrs796052970
Varsomers796052970
Maprs796052970
PheGenIrs796052970
hapmaprs796052970
1000 genomesrs796052970
hgdprs796052970
ensemblrs796052970
gopubmedrs796052970
geneviewrs796052970
scholarrs796052970
googlers796052970
pharmgkbrs796052970
gwascentralrs796052970
openSNPrs796052970
23andMers796052970
23andMe allrs796052970
SNP Nexus

SNPshotrs796052970
SNPdbers796052970
MSV3drs796052970
GWAS Ctlgrs796052970
Max Magnitude0
ClinVar
Risk rs796052970(C;C)
Alt rs796052970(C;C)
Reference rs796052970(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166904213A>G
CLNSRC
CLNACC RCV000188859.1,