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rs397514581

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514581(A;A)
Make rs397514581(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position63444711
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs397514581
ebirs397514581
HLIrs397514581
Exacrs397514581
Varsomers397514581
Maprs397514581
PheGenIrs397514581
hapmaprs397514581
1000 genomesrs397514581
hgdprs397514581
ensemblrs397514581
gopubmedrs397514581
geneviewrs397514581
scholarrs397514581
googlers397514581
pharmgkbrs397514581
gwascentralrs397514581
openSNPrs397514581
23andMers397514581
23andMe allrs397514581
SNP Nexus

SNPshotrs397514581
SNPdbers397514581
MSV3drs397514581
GWAS Ctlgrs397514581
Max Magnitude0
ClinVar
Risk rs397514581(A;A)
Alt rs397514581(A;A)
Reference rs397514581(G;G)
Significance Other
Disease Early infantile epileptic encephalopathy 7 not provided
Variation info
Gene KCNQ2
CLNDBN Early infantile epileptic encephalopathy 7 not provided
Reversed 1
HGVS NC_000020.10:g.62076064C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032979.4, RCV000187867.2,