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rs796053031

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053031(A;A)
Make rs796053031(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992280
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053031
ebirs796053031
HLIrs796053031
Exacrs796053031
Varsomers796053031
Maprs796053031
PheGenIrs796053031
hapmaprs796053031
1000 genomesrs796053031
hgdprs796053031
ensemblrs796053031
gopubmedrs796053031
geneviewrs796053031
scholarrs796053031
googlers796053031
pharmgkbrs796053031
gwascentralrs796053031
openSNPrs796053031
23andMers796053031
23andMe allrs796053031
SNP Nexus

SNPshotrs796053031
SNPdbers796053031
MSV3drs796053031
GWAS Ctlgrs796053031
Max Magnitude0
ClinVar
Risk rs796053031(A;A)
Alt rs796053031(A;A)
Reference rs796053031(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848790C>T
CLNSRC
CLNACC RCV000188989.1,