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rs796052634

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052634(A;A)
Make rs796052634(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63442413
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052634
ebirs796052634
HLIrs796052634
Exacrs796052634
Varsomers796052634
Maprs796052634
PheGenIrs796052634
hapmaprs796052634
1000 genomesrs796052634
hgdprs796052634
ensemblrs796052634
gopubmedrs796052634
geneviewrs796052634
scholarrs796052634
googlers796052634
pharmgkbrs796052634
gwascentralrs796052634
openSNPrs796052634
23andMers796052634
23andMe allrs796052634
SNP Nexus

SNPshotrs796052634
SNPdbers796052634
MSV3drs796052634
GWAS Ctlgrs796052634
Max Magnitude0
ClinVar
Risk rs796052634(A;A)
Alt rs796052634(A;A)
Reference rs796052634(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62073766C>T
CLNSRC
CLNACC RCV000187878.1,