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rs796053098

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053098(A;A)
Make rs796053098(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992144
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053098
ebirs796053098
HLIrs796053098
Exacrs796053098
Varsomers796053098
Maprs796053098
PheGenIrs796053098
hapmaprs796053098
1000 genomesrs796053098
hgdprs796053098
ensemblrs796053098
gopubmedrs796053098
geneviewrs796053098
scholarrs796053098
googlers796053098
pharmgkbrs796053098
gwascentralrs796053098
openSNPrs796053098
23andMers796053098
23andMe allrs796053098
SNP Nexus

SNPshotrs796053098
SNPdbers796053098
MSV3drs796053098
GWAS Ctlgrs796053098
Max Magnitude0
ClinVar
Risk rs796053098(A;A)
Alt rs796053098(A;A)
Reference rs796053098(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848654C>T
CLNSRC
CLNACC RCV000189090.2,