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rs118192201

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118192201(A;G)
Make rs118192201(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position63444727
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs118192201
ebirs118192201
HLIrs118192201
Exacrs118192201
Varsomers118192201
Maprs118192201
PheGenIrs118192201
hapmaprs118192201
1000 genomesrs118192201
hgdprs118192201
ensemblrs118192201
gopubmedrs118192201
geneviewrs118192201
scholarrs118192201
googlers118192201
pharmgkbrs118192201
gwascentralrs118192201
openSNPrs118192201
23andMers118192201
23andMe allrs118192201
SNP Nexus

SNPshotrs118192201
SNPdbers118192201
MSV3drs118192201
GWAS Ctlgrs118192201
Max Magnitude0
ClinVar
Risk rs118192201(G;G)
Alt rs118192201(G;G)
Reference rs118192201(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.62076080T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000021003.1,


OMIM121200
Desc
Variant
Relatedalso