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

rs796053023

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053023(A;A)
Make rs796053023(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165994324
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053023
ebirs796053023
HLIrs796053023
Exacrs796053023
Varsomers796053023
Maprs796053023
PheGenIrs796053023
hapmaprs796053023
1000 genomesrs796053023
hgdprs796053023
ensemblrs796053023
gopubmedrs796053023
geneviewrs796053023
scholarrs796053023
googlers796053023
pharmgkbrs796053023
gwascentralrs796053023
openSNPrs796053023
23andMers796053023
23andMe allrs796053023
SNP Nexus

SNPshotrs796053023
SNPdbers796053023
MSV3drs796053023
GWAS Ctlgrs796053023
Max Magnitude0
ClinVar
Risk rs796053023(A;A)
Alt rs796053023(A;A)
Reference rs796053023(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166850834C>T
CLNSRC
CLNACC RCV000188969.2,