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rs1057524860

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524860(A;G)
Make rs1057524860(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position63438692
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1057524860
dbSNP (old)rs1057524860
ClinGenrs1057524860
ebirs1057524860
HLIrs1057524860
Exacrs1057524860
Gnomadrs1057524860
Varsomers1057524860
Maprs1057524860
PheGenIrs1057524860
Biobankrs1057524860
1000 genomesrs1057524860
hgdprs1057524860
ensemblrs1057524860
gopubmedrs1057524860
geneviewrs1057524860
scholarrs1057524860
googlers1057524860
pharmgkbrs1057524860
gwascentralrs1057524860
openSNPrs1057524860
23andMers1057524860
23andMe allrs1057524860
SNPshotrs1057524860
SNPdbers1057524860
MSV3drs1057524860
GWAS Ctlgrs1057524860
Max Magnitude0
ClinVar
Risk rs1057524860(G;G)
Alt rs1057524860(G;G)
Reference Rs1057524860(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62070045T>C
CLNSRC
CLNACC RCV000437292.1,