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rs1064794686

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome20
Position63414180
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1064794686
dbSNP (old)rs1064794686
ClinGenrs1064794686
ebirs1064794686
HLIrs1064794686
Exacrs1064794686
Gnomadrs1064794686
Varsomers1064794686
Maprs1064794686
PheGenIrs1064794686
Biobankrs1064794686
1000 genomesrs1064794686
hgdprs1064794686
ensemblrs1064794686
gopubmedrs1064794686
geneviewrs1064794686
scholarrs1064794686
googlers1064794686
pharmgkbrs1064794686
gwascentralrs1064794686
openSNPrs1064794686
23andMers1064794686
23andMe allrs1064794686
SNPshotrs1064794686
SNPdbers1064794686
MSV3drs1064794686
GWAS Ctlgrs1064794686
Max Magnitude0
ClinVar
Risk rs1064794686(-;-)
Alt rs1064794686(-;-)
Reference Rs1064794686(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62045533delG
CLNSRC
CLNACC RCV000485046.1,