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rs797044933

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044933(C;T)
Make rs797044933(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165154514
GeneSCN2A, SCN3A
is asnp
is mentioned by
dbSNPrs797044933
ebirs797044933
HLIrs797044933
Exacrs797044933
Varsomers797044933
Maprs797044933
PheGenIrs797044933
hapmaprs797044933
1000 genomesrs797044933
hgdprs797044933
ensemblrs797044933
gopubmedrs797044933
geneviewrs797044933
scholarrs797044933
googlers797044933
pharmgkbrs797044933
gwascentralrs797044933
openSNPrs797044933
23andMers797044933
23andMe allrs797044933
SNP Nexus

SNPshotrs797044933
SNPdbers797044933
MSV3drs797044933
GWAS Ctlgrs797044933
Max Magnitude0
ClinVar
Risk rs797044933(T;T)
Alt rs797044933(T;T)
Reference rs797044933(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SCN2A SCN3A
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000002.11:g.166011024G>A
CLNSRC
CLNACC RCV000190774.1,