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rs796052644

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052644(A;A)
Make rs796052644(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63433848
GeneKCNQ2, LOC105372721
is asnp
is mentioned by
dbSNPrs796052644
ebirs796052644
HLIrs796052644
Exacrs796052644
Varsomers796052644
Maprs796052644
PheGenIrs796052644
hapmaprs796052644
1000 genomesrs796052644
hgdprs796052644
ensemblrs796052644
gopubmedrs796052644
geneviewrs796052644
scholarrs796052644
googlers796052644
pharmgkbrs796052644
gwascentralrs796052644
openSNPrs796052644
23andMers796052644
23andMe allrs796052644
SNP Nexus

SNPshotrs796052644
SNPdbers796052644
MSV3drs796052644
GWAS Ctlgrs796052644
Max Magnitude0
ClinVar
Risk rs796052644(A;A)
Alt rs796052644(A;A)
Reference rs796052644(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62065201C>T
CLNSRC
CLNACC RCV000187892.1,