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

rs796053034

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053034(C;C)
Make rs796053034(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992074
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053034
ebirs796053034
HLIrs796053034
Exacrs796053034
Varsomers796053034
Maprs796053034
PheGenIrs796053034
hapmaprs796053034
1000 genomesrs796053034
hgdprs796053034
ensemblrs796053034
gopubmedrs796053034
geneviewrs796053034
scholarrs796053034
googlers796053034
pharmgkbrs796053034
gwascentralrs796053034
openSNPrs796053034
23andMers796053034
23andMe allrs796053034
SNP Nexus

SNPshotrs796053034
SNPdbers796053034
MSV3drs796053034
GWAS Ctlgrs796053034
Max Magnitude0
ClinVar
Risk rs796053034(C;C)
Alt rs796053034(C;C)
Reference rs796053034(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848584A>G
CLNSRC
CLNACC RCV000188994.1,