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rs796052623

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052623(C;T)
Make rs796052623(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63444748
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052623
ebirs796052623
HLIrs796052623
Exacrs796052623
Varsomers796052623
Maprs796052623
PheGenIrs796052623
hapmaprs796052623
1000 genomesrs796052623
hgdprs796052623
ensemblrs796052623
gopubmedrs796052623
geneviewrs796052623
scholarrs796052623
googlers796052623
pharmgkbrs796052623
gwascentralrs796052623
openSNPrs796052623
23andMers796052623
23andMe allrs796052623
SNP Nexus

SNPshotrs796052623
SNPdbers796052623
MSV3drs796052623
GWAS Ctlgrs796052623
Max Magnitude0
ClinVar
Risk rs796052623(T;T)
Alt rs796052623(T;T)
Reference rs796052623(C;C)
Significance Pathogenic
Disease not provided Early infantile epileptic encephalopathy 7
Variation info
Gene KCNQ2
CLNDBN not provided Early infantile epileptic encephalopathy 7
Reversed 1
HGVS NC_000020.10:g.62076101G>A
CLNSRC
CLNACC RCV000187858.2, RCV000203591.1,