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rs796053002

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053002(A;A)
Make rs796053002(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166009803
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053002
ebirs796053002
HLIrs796053002
Exacrs796053002
Varsomers796053002
Maprs796053002
PheGenIrs796053002
hapmaprs796053002
1000 genomesrs796053002
hgdprs796053002
ensemblrs796053002
gopubmedrs796053002
geneviewrs796053002
scholarrs796053002
googlers796053002
pharmgkbrs796053002
gwascentralrs796053002
openSNPrs796053002
23andMers796053002
23andMe allrs796053002
SNP Nexus

SNPshotrs796053002
SNPdbers796053002
MSV3drs796053002
GWAS Ctlgrs796053002
Max Magnitude0
ClinVar
Risk rs796053002(A;A)
Alt rs796053002(A;A)
Reference rs796053002(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166866313G>T
CLNSRC
CLNACC RCV000188934.1,