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rs796052620

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052620(C;C)
Make rs796052620(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63444766
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052620
ebirs796052620
HLIrs796052620
Exacrs796052620
Varsomers796052620
Maprs796052620
PheGenIrs796052620
hapmaprs796052620
1000 genomesrs796052620
hgdprs796052620
ensemblrs796052620
gopubmedrs796052620
geneviewrs796052620
scholarrs796052620
googlers796052620
pharmgkbrs796052620
gwascentralrs796052620
openSNPrs796052620
23andMers796052620
23andMe allrs796052620
SNP Nexus

SNPshotrs796052620
SNPdbers796052620
MSV3drs796052620
GWAS Ctlgrs796052620
Max Magnitude0
ClinVar
Risk rs796052620(C;C)
Alt rs796052620(C;C)
Reference rs796052620(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62076119A>G
CLNSRC
CLNACC RCV000187855.2,