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rs796053032

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053032(C;T)
Make rs796053032(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992276
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053032
ebirs796053032
HLIrs796053032
Exacrs796053032
Varsomers796053032
Maprs796053032
PheGenIrs796053032
hapmaprs796053032
1000 genomesrs796053032
hgdprs796053032
ensemblrs796053032
gopubmedrs796053032
geneviewrs796053032
scholarrs796053032
googlers796053032
pharmgkbrs796053032
gwascentralrs796053032
openSNPrs796053032
23andMers796053032
23andMe allrs796053032
SNP Nexus

SNPshotrs796053032
SNPdbers796053032
MSV3drs796053032
GWAS Ctlgrs796053032
Max Magnitude0
ClinVar
Risk rs796053032(T;T)
Alt rs796053032(T;T)
Reference rs796053032(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848786G>A
CLNSRC
CLNACC RCV000188990.2,