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rs1057523728

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057523728(A;A)
Make rs1057523728(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position63439692
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1057523728
dbSNP (old)rs1057523728
ClinGenrs1057523728
ebirs1057523728
HLIrs1057523728
Exacrs1057523728
Gnomadrs1057523728
Varsomers1057523728
LitVarrs1057523728
Maprs1057523728
PheGenIrs1057523728
Biobankrs1057523728
1000 genomesrs1057523728
hgdprs1057523728
ensemblrs1057523728
gopubmedrs1057523728
geneviewrs1057523728
scholarrs1057523728
googlers1057523728
pharmgkbrs1057523728
gwascentralrs1057523728
openSNPrs1057523728
23andMers1057523728
23andMe allrs1057523728
SNPshotrs1057523728
SNPdbers1057523728
MSV3drs1057523728
GWAS Ctlgrs1057523728
Max Magnitude0
ClinVar
Risk rs1057523728(A;A)
Alt rs1057523728(A;A)
Reference Rs1057523728(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62071045A>G; NC_000020.10:g.62071045A>T
CLNSRC
CLNACC RCV000494098.1, RCV000437231.1,