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rs397507449

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507449(A;A)
Make rs397507449(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position63433808
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs397507449
ebirs397507449
HLIrs397507449
Exacrs397507449
Varsomers397507449
Maprs397507449
PheGenIrs397507449
hapmaprs397507449
1000 genomesrs397507449
hgdprs397507449
ensemblrs397507449
gopubmedrs397507449
geneviewrs397507449
scholarrs397507449
googlers397507449
pharmgkbrs397507449
gwascentralrs397507449
openSNPrs397507449
23andMers397507449
23andMe allrs397507449
SNP Nexus

SNPshotrs397507449
SNPdbers397507449
MSV3drs397507449
GWAS Ctlgrs397507449
Max Magnitude0
ClinVar
Risk rs397507449(A;A)
Alt rs397507449(A;A)
Reference rs397507449(G;G)
Significance Pathogenic
Disease Benign familial neonatal seizures 1
Variation info
Gene KCNQ2
CLNDBN Benign familial neonatal seizures 1
Reversed 1
HGVS NC_000020.10:g.62065161C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000020966.2,