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rs1064796535

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome20
Position63438662
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1064796535
dbSNP (old)rs1064796535
ClinGenrs1064796535
ebirs1064796535
HLIrs1064796535
Exacrs1064796535
Gnomadrs1064796535
Varsomers1064796535
Maprs1064796535
PheGenIrs1064796535
Biobankrs1064796535
1000 genomesrs1064796535
hgdprs1064796535
ensemblrs1064796535
gopubmedrs1064796535
geneviewrs1064796535
scholarrs1064796535
googlers1064796535
pharmgkbrs1064796535
gwascentralrs1064796535
openSNPrs1064796535
23andMers1064796535
23andMe allrs1064796535
SNPshotrs1064796535
SNPdbers1064796535
MSV3drs1064796535
GWAS Ctlgrs1064796535
Max Magnitude0
ClinVar
Risk rs1064796535(C;C)
Alt rs1064796535(C;C)
Reference Rs1064796535(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62070015A>G
CLNSRC
CLNACC RCV000487056.1,