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

rs796053070

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053070(-;-)
Make rs796053070(-;A)
Make rs796053070(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166036208
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053070
ebirs796053070
HLIrs796053070
Exacrs796053070
Varsomers796053070
Maprs796053070
PheGenIrs796053070
hapmaprs796053070
1000 genomesrs796053070
hgdprs796053070
ensemblrs796053070
gopubmedrs796053070
geneviewrs796053070
scholarrs796053070
googlers796053070
pharmgkbrs796053070
gwascentralrs796053070
openSNPrs796053070
23andMers796053070
23andMe allrs796053070
SNP Nexus

SNPshotrs796053070
SNPdbers796053070
MSV3drs796053070
GWAS Ctlgrs796053070
Max Magnitude0
ClinVar
Risk rs796053070(A;A)
Alt rs796053070(A;A)
Reference rs796053070(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166892719dupT
CLNSRC
CLNACC RCV000189050.1,