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

rs796053039

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053039(G;T)
Make rs796053039(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991859
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053039
ebirs796053039
HLIrs796053039
Exacrs796053039
Varsomers796053039
Maprs796053039
PheGenIrs796053039
hapmaprs796053039
1000 genomesrs796053039
hgdprs796053039
ensemblrs796053039
gopubmedrs796053039
geneviewrs796053039
scholarrs796053039
googlers796053039
pharmgkbrs796053039
gwascentralrs796053039
openSNPrs796053039
23andMers796053039
23andMe allrs796053039
SNP Nexus

SNPshotrs796053039
SNPdbers796053039
MSV3drs796053039
GWAS Ctlgrs796053039
Max Magnitude0
ClinVar
Risk rs796053039(T;T)
Alt rs796053039(T;T)
Reference rs796053039(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848369C>A
CLNSRC
CLNACC RCV000189002.1,