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rs796052960

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052960(C;C)
Make rs796052960(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166052890
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052960
ebirs796052960
HLIrs796052960
Exacrs796052960
Varsomers796052960
Maprs796052960
PheGenIrs796052960
hapmaprs796052960
1000 genomesrs796052960
hgdprs796052960
ensemblrs796052960
gopubmedrs796052960
geneviewrs796052960
scholarrs796052960
googlers796052960
pharmgkbrs796052960
gwascentralrs796052960
openSNPrs796052960
23andMers796052960
23andMe allrs796052960
SNP Nexus

SNPshotrs796052960
SNPdbers796052960
MSV3drs796052960
GWAS Ctlgrs796052960
Max Magnitude0
ClinVar
Risk rs796052960(C;C)
Alt rs796052960(C;C)
Reference rs796052960(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166909400C>G
CLNSRC
CLNACC RCV000188839.1,