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rs118192209

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118192209(G;T)
Make rs118192209(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position63442410
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs118192209
ebirs118192209
HLIrs118192209
Exacrs118192209
Varsomers118192209
Maprs118192209
PheGenIrs118192209
hapmaprs118192209
1000 genomesrs118192209
hgdprs118192209
ensemblrs118192209
gopubmedrs118192209
geneviewrs118192209
scholarrs118192209
googlers118192209
pharmgkbrs118192209
gwascentralrs118192209
openSNPrs118192209
23andMers118192209
23andMe allrs118192209
SNP Nexus

SNPshotrs118192209
SNPdbers118192209
MSV3drs118192209
GWAS Ctlgrs118192209
Max Magnitude0
ClinVar
Risk rs118192209(T;T)
Alt rs118192209(T;T)
Reference rs118192209(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.62073763C>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000021013.1,


OMIM121200
Desc
Variant
Relatedalso