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rs796052955

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052955(C;T)
Make rs796052955(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166058642
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052955
dbSNP (old)rs796052955
ClinGenrs796052955
ebirs796052955
HLIrs796052955
Exacrs796052955
Gnomadrs796052955
Varsomers796052955
Maprs796052955
PheGenIrs796052955
Biobankrs796052955
1000 genomesrs796052955
hgdprs796052955
ensemblrs796052955
gopubmedrs796052955
geneviewrs796052955
scholarrs796052955
googlers796052955
pharmgkbrs796052955
gwascentralrs796052955
openSNPrs796052955
23andMers796052955
23andMe allrs796052955
SNP Nexus

SNPshotrs796052955
SNPdbers796052955
MSV3drs796052955
GWAS Ctlgrs796052955
Max Magnitude0
ClinVar
Risk rs796052955(T;T)
Alt rs796052955(T;T)
Reference Rs796052955(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166915152G>A
CLNSRC
CLNACC RCV000188830.1,