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

rs796053030

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053030(A;A)
Make rs796053030(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992344
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053030
ebirs796053030
HLIrs796053030
Exacrs796053030
Varsomers796053030
Maprs796053030
PheGenIrs796053030
hapmaprs796053030
1000 genomesrs796053030
hgdprs796053030
ensemblrs796053030
gopubmedrs796053030
geneviewrs796053030
scholarrs796053030
googlers796053030
pharmgkbrs796053030
gwascentralrs796053030
openSNPrs796053030
23andMers796053030
23andMe allrs796053030
SNP Nexus

SNPshotrs796053030
SNPdbers796053030
MSV3drs796053030
GWAS Ctlgrs796053030
Max Magnitude0
ClinVar
Risk rs796053030(A;A)
Alt rs796053030(A;A)
Reference rs796053030(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848854C>T
CLNSRC
CLNACC RCV000188985.2,