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

rs796053051

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053051(-;-)
Make rs796053051(-;T)
Make rs796053051(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166058647
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053051
ebirs796053051
HLIrs796053051
Exacrs796053051
Varsomers796053051
Maprs796053051
PheGenIrs796053051
hapmaprs796053051
1000 genomesrs796053051
hgdprs796053051
ensemblrs796053051
gopubmedrs796053051
geneviewrs796053051
scholarrs796053051
googlers796053051
pharmgkbrs796053051
gwascentralrs796053051
openSNPrs796053051
23andMers796053051
23andMe allrs796053051
SNP Nexus

SNPshotrs796053051
SNPdbers796053051
MSV3drs796053051
GWAS Ctlgrs796053051
Max Magnitude0
ClinVar
Risk rs796053051(T;T)
Alt rs796053051(T;T)
Reference rs796053051(;)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166915158dupA
CLNSRC
CLNACC RCV000189031.1,