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rs796052958

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052958(A;A)
Make rs796052958(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166054638
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052958
ebirs796052958
HLIrs796052958
Exacrs796052958
Varsomers796052958
Maprs796052958
PheGenIrs796052958
hapmaprs796052958
1000 genomesrs796052958
hgdprs796052958
ensemblrs796052958
gopubmedrs796052958
geneviewrs796052958
scholarrs796052958
googlers796052958
pharmgkbrs796052958
gwascentralrs796052958
openSNPrs796052958
23andMers796052958
23andMe allrs796052958
SNP Nexus

SNPshotrs796052958
SNPdbers796052958
MSV3drs796052958
GWAS Ctlgrs796052958
Max Magnitude0
ClinVar
Risk rs796052958(A;A)
Alt rs796052958(A;A)
Reference rs796052958(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166911148G>T
CLNSRC
CLNACC RCV000188836.1,