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rs1064795435

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CCT;CCT) 0 common in clinvar
Chromosome20
Position63446829
GeneKCNQ2, LOC105372720
is asnp
is mentioned by
dbSNPrs1064795435
dbSNP (old)rs1064795435
ClinGenrs1064795435
ebirs1064795435
HLIrs1064795435
Exacrs1064795435
Gnomadrs1064795435
Varsomers1064795435
Maprs1064795435
PheGenIrs1064795435
Biobankrs1064795435
1000 genomesrs1064795435
hgdprs1064795435
ensemblrs1064795435
gopubmedrs1064795435
geneviewrs1064795435
scholarrs1064795435
googlers1064795435
pharmgkbrs1064795435
gwascentralrs1064795435
openSNPrs1064795435
23andMers1064795435
23andMe allrs1064795435
SNPshotrs1064795435
SNPdbers1064795435
MSV3drs1064795435
GWAS Ctlgrs1064795435
Max Magnitude0
ClinVar
Risk rs1064795435(-;-)
Alt rs1064795435(-;-)
Reference Rs1064795435(CCT;CCT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62078182_62078184delAGG
CLNSRC
CLNACC RCV000486606.1,