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rs796052982

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052982(A;A)
Make rs796052982(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166039443
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052982
ebirs796052982
HLIrs796052982
Exacrs796052982
Varsomers796052982
Maprs796052982
PheGenIrs796052982
hapmaprs796052982
1000 genomesrs796052982
hgdprs796052982
ensemblrs796052982
gopubmedrs796052982
geneviewrs796052982
scholarrs796052982
googlers796052982
pharmgkbrs796052982
gwascentralrs796052982
openSNPrs796052982
23andMers796052982
23andMe allrs796052982
SNP Nexus

SNPshotrs796052982
SNPdbers796052982
MSV3drs796052982
GWAS Ctlgrs796052982
Max Magnitude0
ClinVar
Risk rs796052982(A;A)
Alt rs796052982(A;A)
Reference rs796052982(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166895953C>T
CLNSRC
CLNACC RCV000188892.1,