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rs1064793334

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome20
Position63433852
GeneKCNQ2, LOC105372721
is asnp
is mentioned by
dbSNPrs1064793334
dbSNP (old)rs1064793334
ClinGenrs1064793334
ebirs1064793334
HLIrs1064793334
Exacrs1064793334
Gnomadrs1064793334
Varsomers1064793334
Maprs1064793334
PheGenIrs1064793334
Biobankrs1064793334
1000 genomesrs1064793334
hgdprs1064793334
ensemblrs1064793334
gopubmedrs1064793334
geneviewrs1064793334
scholarrs1064793334
googlers1064793334
pharmgkbrs1064793334
gwascentralrs1064793334
openSNPrs1064793334
23andMers1064793334
23andMe allrs1064793334
SNPshotrs1064793334
SNPdbers1064793334
MSV3drs1064793334
GWAS Ctlgrs1064793334
Max Magnitude0
ClinVar
Risk rs1064793334(G;G)
Alt rs1064793334(G;G)
Reference Rs1064793334(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62065205T>C
CLNSRC
CLNACC RCV000478942.1,