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rs118192237

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118192237(A;T)
Make rs118192237(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position63408536
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs118192237
ebirs118192237
HLIrs118192237
Exacrs118192237
Varsomers118192237
Maprs118192237
PheGenIrs118192237
hapmaprs118192237
1000 genomesrs118192237
hgdprs118192237
ensemblrs118192237
gopubmedrs118192237
geneviewrs118192237
scholarrs118192237
googlers118192237
pharmgkbrs118192237
gwascentralrs118192237
openSNPrs118192237
23andMers118192237
23andMe allrs118192237
SNP Nexus

SNPshotrs118192237
SNPdbers118192237
MSV3drs118192237
GWAS Ctlgrs118192237
Max Magnitude0
ClinVar
Risk rs118192237(T;T)
Alt rs118192237(T;T)
Reference rs118192237(A;A)
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.62039889T>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000020978.1,


OMIM121200
Desc
Variant
Relatedalso