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rs796053048

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053048(C;T)
Make rs796053048(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991522
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053048
ebirs796053048
HLIrs796053048
Exacrs796053048
Varsomers796053048
Maprs796053048
PheGenIrs796053048
hapmaprs796053048
1000 genomesrs796053048
hgdprs796053048
ensemblrs796053048
gopubmedrs796053048
geneviewrs796053048
scholarrs796053048
googlers796053048
pharmgkbrs796053048
gwascentralrs796053048
openSNPrs796053048
23andMers796053048
23andMe allrs796053048
SNP Nexus

SNPshotrs796053048
SNPdbers796053048
MSV3drs796053048
GWAS Ctlgrs796053048
Max Magnitude0
ClinVar
Risk rs796053048(T;T)
Alt rs796053048(T;T)
Reference rs796053048(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848032G>A
CLNSRC
CLNACC RCV000189019.2,