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rs796053001

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053001(C;C)
Make rs796053001(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166012138
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053001
ebirs796053001
HLIrs796053001
Exacrs796053001
Varsomers796053001
Maprs796053001
PheGenIrs796053001
hapmaprs796053001
1000 genomesrs796053001
hgdprs796053001
ensemblrs796053001
gopubmedrs796053001
geneviewrs796053001
scholarrs796053001
googlers796053001
pharmgkbrs796053001
gwascentralrs796053001
openSNPrs796053001
23andMers796053001
23andMe allrs796053001
SNP Nexus

SNPshotrs796053001
SNPdbers796053001
MSV3drs796053001
GWAS Ctlgrs796053001
Max Magnitude0
ClinVar
Risk rs796053001(C;C)
Alt rs796053001(C;C)
Reference rs796053001(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166868648A>G
CLNSRC
CLNACC RCV000188932.1,