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

rs118192210

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs118192210(-;-)
Make rs118192210(-;GT)
Make rs118192210(GT;GT)
ReferenceGRCh38 38.1/141
Chromosome20
Position63439677
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs118192210
ebirs118192210
HLIrs118192210
Exacrs118192210
Varsomers118192210
Maprs118192210
PheGenIrs118192210
hapmaprs118192210
1000 genomesrs118192210
hgdprs118192210
ensemblrs118192210
gopubmedrs118192210
geneviewrs118192210
scholarrs118192210
googlers118192210
pharmgkbrs118192210
gwascentralrs118192210
openSNPrs118192210
23andMers118192210
23andMe allrs118192210
SNP Nexus

SNPshotrs118192210
SNPdbers118192210
MSV3drs118192210
GWAS Ctlgrs118192210
Max Magnitude0
ClinVar
Risk rs118192210(GT;GT)
Alt rs118192210(GT;GT)
Reference rs118192210(;)
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.62071030_62071031insAC
CLNSRC ClinVar GeneReviews
CLNACC RCV000021014.1,


OMIM121200
Desc
Variant
Relatedalso