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rs797044935

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044935(A;G)
Make rs797044935(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63442512
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs797044935
ebirs797044935
HLIrs797044935
Exacrs797044935
Varsomers797044935
Maprs797044935
PheGenIrs797044935
hapmaprs797044935
1000 genomesrs797044935
hgdprs797044935
ensemblrs797044935
gopubmedrs797044935
geneviewrs797044935
scholarrs797044935
googlers797044935
pharmgkbrs797044935
gwascentralrs797044935
openSNPrs797044935
23andMers797044935
23andMe allrs797044935
SNP Nexus

SNPshotrs797044935
SNPdbers797044935
MSV3drs797044935
GWAS Ctlgrs797044935
Max Magnitude0
ClinVar
Risk rs797044935(G;G)
Alt rs797044935(G;G)
Reference rs797044935(A;A)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene KCNQ2
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000020.10:g.62073865T>C
CLNSRC
CLNACC RCV000190778.1,