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rs796053037

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053037(A;A)
Make rs796053037(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991984
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053037
ebirs796053037
HLIrs796053037
Exacrs796053037
Varsomers796053037
Maprs796053037
PheGenIrs796053037
hapmaprs796053037
1000 genomesrs796053037
hgdprs796053037
ensemblrs796053037
gopubmedrs796053037
geneviewrs796053037
scholarrs796053037
googlers796053037
pharmgkbrs796053037
gwascentralrs796053037
openSNPrs796053037
23andMers796053037
23andMe allrs796053037
SNP Nexus

SNPshotrs796053037
SNPdbers796053037
MSV3drs796053037
GWAS Ctlgrs796053037
Max Magnitude0
ClinVar
Risk rs796053037(A;A)
Alt rs796053037(A;A)
Reference rs796053037(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848494A>T
CLNSRC
CLNACC RCV000188998.1,