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

rs794727741

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727741(C;T)
Make rs794727741(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63442521
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs794727741
ebirs794727741
HLIrs794727741
Exacrs794727741
Varsomers794727741
Maprs794727741
PheGenIrs794727741
hapmaprs794727741
1000 genomesrs794727741
hgdprs794727741
ensemblrs794727741
gopubmedrs794727741
geneviewrs794727741
scholarrs794727741
googlers794727741
pharmgkbrs794727741
gwascentralrs794727741
openSNPrs794727741
23andMers794727741
23andMe allrs794727741
SNP Nexus

SNPshotrs794727741
SNPdbers794727741
MSV3drs794727741
GWAS Ctlgrs794727741
Max Magnitude0
ClinVar
Risk rs794727741(T;T)
Alt rs794727741(T;T)
Reference rs794727741(C;C)
Significance Probable-Pathogenic
Disease not provided Seizures
Variation info
Gene KCNQ2
CLNDBN not provided Seizures
Reversed 1
HGVS NC_000020.10:g.62073874G>A
CLNSRC
CLNACC RCV000179033.1, RCV000193491.1,