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rs796053045

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053045(A;A)
Make rs796053045(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991532
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053045
ebirs796053045
HLIrs796053045
Exacrs796053045
Varsomers796053045
Maprs796053045
PheGenIrs796053045
hapmaprs796053045
1000 genomesrs796053045
hgdprs796053045
ensemblrs796053045
gopubmedrs796053045
geneviewrs796053045
scholarrs796053045
googlers796053045
pharmgkbrs796053045
gwascentralrs796053045
openSNPrs796053045
23andMers796053045
23andMe allrs796053045
SNP Nexus

SNPshotrs796053045
SNPdbers796053045
MSV3drs796053045
GWAS Ctlgrs796053045
Max Magnitude0
ClinVar
Risk rs796053045(A;A)
Alt rs796053045(A;A)
Reference rs796053045(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848042C>T
CLNSRC
CLNACC RCV000189016.2,