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rs796053018

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053018(A;T)
Make rs796053018(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165996083
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053018
ebirs796053018
HLIrs796053018
Exacrs796053018
Varsomers796053018
Maprs796053018
PheGenIrs796053018
hapmaprs796053018
1000 genomesrs796053018
hgdprs796053018
ensemblrs796053018
gopubmedrs796053018
geneviewrs796053018
scholarrs796053018
googlers796053018
pharmgkbrs796053018
gwascentralrs796053018
openSNPrs796053018
23andMers796053018
23andMe allrs796053018
SNP Nexus

SNPshotrs796053018
SNPdbers796053018
MSV3drs796053018
GWAS Ctlgrs796053018
Max Magnitude0
ClinVar
Risk rs796053018(T;T)
Alt rs796053018(T;T)
Reference rs796053018(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166852593T>A
CLNSRC
CLNACC RCV000188958.2,