Have questions? Visit https://www.reddit.com/r/SNPedia

rs118192206

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs118192206(G;G)
Make rs118192206(G;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position63442473
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs118192206
ebirs118192206
HLIrs118192206
Exacrs118192206
Varsomers118192206
Maprs118192206
PheGenIrs118192206
hapmaprs118192206
1000 genomesrs118192206
hgdprs118192206
ensemblrs118192206
gopubmedrs118192206
geneviewrs118192206
scholarrs118192206
googlers118192206
pharmgkbrs118192206
gwascentralrs118192206
openSNPrs118192206
23andMers118192206
23andMe allrs118192206
SNP Nexus

SNPshotrs118192206
SNPdbers118192206
MSV3drs118192206
GWAS Ctlgrs118192206
Max Magnitude0
ClinVar
Risk rs118192206(G;G)
Alt rs118192206(G;G)
Reference rs118192206(T;T)
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.62073826A>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000021010.1,


OMIM121200
Desc
Variant
Relatedalso