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rs1064796151

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTGT;CTGT) 0 common in clinvar
Chromosome20
Position63446802
GeneKCNQ2, LOC105372720
is asnp
is mentioned by
dbSNPrs1064796151
dbSNP (old)rs1064796151
ClinGenrs1064796151
ebirs1064796151
HLIrs1064796151
Exacrs1064796151
Gnomadrs1064796151
Varsomers1064796151
LitVarrs1064796151
Maprs1064796151
PheGenIrs1064796151
Biobankrs1064796151
1000 genomesrs1064796151
hgdprs1064796151
ensemblrs1064796151
gopubmedrs1064796151
geneviewrs1064796151
scholarrs1064796151
googlers1064796151
pharmgkbrs1064796151
gwascentralrs1064796151
openSNPrs1064796151
23andMers1064796151
23andMe allrs1064796151
SNPshotrs1064796151
SNPdbers1064796151
MSV3drs1064796151
GWAS Ctlgrs1064796151
Max Magnitude0
ClinVar
Risk rs1064796151(-;-)
Alt rs1064796151(-;-)
Reference Rs1064796151(CTGT;CTGT)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62078155_62078158delACAG
CLNSRC
CLNACC RCV000480357.1,