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

rs797044952

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044952(A;C)
Make rs797044952(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166002743
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs797044952
ebirs797044952
HLIrs797044952
Exacrs797044952
Varsomers797044952
Maprs797044952
PheGenIrs797044952
hapmaprs797044952
1000 genomesrs797044952
hgdprs797044952
ensemblrs797044952
gopubmedrs797044952
geneviewrs797044952
scholarrs797044952
googlers797044952
pharmgkbrs797044952
gwascentralrs797044952
openSNPrs797044952
23andMers797044952
23andMe allrs797044952
SNP Nexus

SNPshotrs797044952
SNPdbers797044952
MSV3drs797044952
GWAS Ctlgrs797044952
Max Magnitude0
ClinVar
Risk rs797044952(C;C)
Alt rs797044952(C;C)
Reference rs797044952(A;A)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene LOC102724058 SCN1A
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000002.11:g.166859253T>G
CLNSRC
CLNACC RCV000190804.1,