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rs796052957

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052957(C;C)
Make rs796052957(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166054735
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052957
ebirs796052957
HLIrs796052957
Exacrs796052957
Varsomers796052957
Maprs796052957
PheGenIrs796052957
hapmaprs796052957
1000 genomesrs796052957
hgdprs796052957
ensemblrs796052957
gopubmedrs796052957
geneviewrs796052957
scholarrs796052957
googlers796052957
pharmgkbrs796052957
gwascentralrs796052957
openSNPrs796052957
23andMers796052957
23andMe allrs796052957
SNP Nexus

SNPshotrs796052957
SNPdbers796052957
MSV3drs796052957
GWAS Ctlgrs796052957
Max Magnitude0
ClinVar
Risk rs796052957(C;C)
Alt rs796052957(C;C)
Reference rs796052957(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166911245A>G
CLNSRC
CLNACC RCV000188835.1,