Have questions? Visit https://www.reddit.com/r/SNPedia

rs796053015

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053015(G;T)
Make rs796053015(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165998076
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053015
ebirs796053015
HLIrs796053015
Exacrs796053015
Varsomers796053015
Maprs796053015
PheGenIrs796053015
hapmaprs796053015
1000 genomesrs796053015
hgdprs796053015
ensemblrs796053015
gopubmedrs796053015
geneviewrs796053015
scholarrs796053015
googlers796053015
pharmgkbrs796053015
gwascentralrs796053015
openSNPrs796053015
23andMers796053015
23andMe allrs796053015
SNP Nexus

SNPshotrs796053015
SNPdbers796053015
MSV3drs796053015
GWAS Ctlgrs796053015
Max Magnitude0
ClinVar
Risk rs796053015(T;T)
Alt rs796053015(T;T)
Reference rs796053015(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166854586C>A
CLNSRC
CLNACC RCV000188954.1,