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rs796053103

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053103(C;T)
Make rs796053103(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991565
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053103
ebirs796053103
HLIrs796053103
Exacrs796053103
Varsomers796053103
Maprs796053103
PheGenIrs796053103
hapmaprs796053103
1000 genomesrs796053103
hgdprs796053103
ensemblrs796053103
gopubmedrs796053103
geneviewrs796053103
scholarrs796053103
googlers796053103
pharmgkbrs796053103
gwascentralrs796053103
openSNPrs796053103
23andMers796053103
23andMe allrs796053103
SNP Nexus

SNPshotrs796053103
SNPdbers796053103
MSV3drs796053103
GWAS Ctlgrs796053103
Max Magnitude0
ClinVar
Risk rs796053103(T;T)
Alt rs796053103(T;T)
Reference rs796053103(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848075G>A
CLNSRC
CLNACC RCV000189095.1,