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rs1064795489

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome20
Position63439683
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1064795489
dbSNP (old)rs1064795489
ClinGenrs1064795489
ebirs1064795489
HLIrs1064795489
Exacrs1064795489
Gnomadrs1064795489
Varsomers1064795489
Maprs1064795489
PheGenIrs1064795489
Biobankrs1064795489
1000 genomesrs1064795489
hgdprs1064795489
ensemblrs1064795489
gopubmedrs1064795489
geneviewrs1064795489
scholarrs1064795489
googlers1064795489
pharmgkbrs1064795489
gwascentralrs1064795489
openSNPrs1064795489
23andMers1064795489
23andMe allrs1064795489
SNPshotrs1064795489
SNPdbers1064795489
MSV3drs1064795489
GWAS Ctlgrs1064795489
Max Magnitude0
ClinVar
Risk rs1064795489(A;A)
Alt rs1064795489(A;A)
Reference Rs1064795489(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62071036C>T
CLNSRC
CLNACC RCV000484620.1,