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

rs796053099

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053099(C;T)
Make rs796053099(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992107
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053099
ebirs796053099
HLIrs796053099
Exacrs796053099
Varsomers796053099
Maprs796053099
PheGenIrs796053099
hapmaprs796053099
1000 genomesrs796053099
hgdprs796053099
ensemblrs796053099
gopubmedrs796053099
geneviewrs796053099
scholarrs796053099
googlers796053099
pharmgkbrs796053099
gwascentralrs796053099
openSNPrs796053099
23andMers796053099
23andMe allrs796053099
SNP Nexus

SNPshotrs796053099
SNPdbers796053099
MSV3drs796053099
GWAS Ctlgrs796053099
Max Magnitude0
ClinVar
Risk rs796053099(T;T)
Alt rs796053099(T;T)
Reference rs796053099(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848617G>A
CLNSRC
CLNACC RCV000189091.2,