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

rs796053046

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053046(G;T)
Make rs796053046(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991529
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053046
ebirs796053046
HLIrs796053046
Exacrs796053046
Varsomers796053046
Maprs796053046
PheGenIrs796053046
hapmaprs796053046
1000 genomesrs796053046
hgdprs796053046
ensemblrs796053046
gopubmedrs796053046
geneviewrs796053046
scholarrs796053046
googlers796053046
pharmgkbrs796053046
gwascentralrs796053046
openSNPrs796053046
23andMers796053046
23andMe allrs796053046
SNP Nexus

SNPshotrs796053046
SNPdbers796053046
MSV3drs796053046
GWAS Ctlgrs796053046
Max Magnitude0
ClinVar
Risk rs796053046(T;T)
Alt rs796053046(T;T)
Reference rs796053046(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848039C>A
CLNSRC
CLNACC RCV000189017.1,