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rs796053020

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053020(A;A)
Make rs796053020(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165996051
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053020
ebirs796053020
HLIrs796053020
Exacrs796053020
Varsomers796053020
Maprs796053020
PheGenIrs796053020
hapmaprs796053020
1000 genomesrs796053020
hgdprs796053020
ensemblrs796053020
gopubmedrs796053020
geneviewrs796053020
scholarrs796053020
googlers796053020
pharmgkbrs796053020
gwascentralrs796053020
openSNPrs796053020
23andMers796053020
23andMe allrs796053020
SNP Nexus

SNPshotrs796053020
SNPdbers796053020
MSV3drs796053020
GWAS Ctlgrs796053020
Max Magnitude0
ClinVar
Risk rs796053020(A;A)
Alt rs796053020(A;A)
Reference rs796053020(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166852561C>T
CLNSRC
CLNACC RCV000188960.1,