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

rs796052622

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052622(C;C)
Make rs796052622(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63444750
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052622
ebirs796052622
HLIrs796052622
Exacrs796052622
Varsomers796052622
Maprs796052622
PheGenIrs796052622
hapmaprs796052622
1000 genomesrs796052622
hgdprs796052622
ensemblrs796052622
gopubmedrs796052622
geneviewrs796052622
scholarrs796052622
googlers796052622
pharmgkbrs796052622
gwascentralrs796052622
openSNPrs796052622
23andMers796052622
23andMe allrs796052622
SNP Nexus

SNPshotrs796052622
SNPdbers796052622
MSV3drs796052622
GWAS Ctlgrs796052622
Max Magnitude0
ClinVar
Risk rs796052622(C;C)
Alt rs796052622(C;C)
Reference rs796052622(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62076103A>G
CLNSRC
CLNACC RCV000187857.1,