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rs1057518489

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518489(A;G)
Make rs1057518489(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position63442446
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1057518489
dbSNP (old)rs1057518489
ClinGenrs1057518489
ebirs1057518489
HLIrs1057518489
Exacrs1057518489
Gnomadrs1057518489
Varsomers1057518489
Maprs1057518489
PheGenIrs1057518489
Biobankrs1057518489
1000 genomesrs1057518489
hgdprs1057518489
ensemblrs1057518489
gopubmedrs1057518489
geneviewrs1057518489
scholarrs1057518489
googlers1057518489
pharmgkbrs1057518489
gwascentralrs1057518489
openSNPrs1057518489
23andMers1057518489
23andMe allrs1057518489
SNPshotrs1057518489
SNPdbers1057518489
MSV3drs1057518489
GWAS Ctlgrs1057518489
Max Magnitude0
ClinVar
Risk rs1057518489(G;G)
Alt rs1057518489(G;G)
Reference Rs1057518489(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62073799T>C
CLNSRC
CLNACC RCV000412840.1,