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rs796053021

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053021(A;A)
Make rs796053021(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165996039
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053021
ebirs796053021
HLIrs796053021
Exacrs796053021
Varsomers796053021
Maprs796053021
PheGenIrs796053021
hapmaprs796053021
1000 genomesrs796053021
hgdprs796053021
ensemblrs796053021
gopubmedrs796053021
geneviewrs796053021
scholarrs796053021
googlers796053021
pharmgkbrs796053021
gwascentralrs796053021
openSNPrs796053021
23andMers796053021
23andMe allrs796053021
SNP Nexus

SNPshotrs796053021
SNPdbers796053021
MSV3drs796053021
GWAS Ctlgrs796053021
Max Magnitude0
ClinVar
Risk rs796053021(A;A)
Alt rs796053021(A;A)
Reference rs796053021(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166852549G>T
CLNSRC
CLNACC RCV000188963.1,