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rs1057519124

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519124(A;A)
Make rs1057519124(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position63442405
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1057519124
dbSNP (classic)rs1057519124
ClinGenrs1057519124
ebirs1057519124
HLIrs1057519124
Exacrs1057519124
Gnomadrs1057519124
Varsomers1057519124
LitVarrs1057519124
Maprs1057519124
PheGenIrs1057519124
Biobankrs1057519124
1000 genomesrs1057519124
hgdprs1057519124
ensemblrs1057519124
geneviewrs1057519124
scholarrs1057519124
googlers1057519124
pharmgkbrs1057519124
gwascentralrs1057519124
openSNPrs1057519124
23andMers1057519124
23andMe allrs1057519124
SNPshotrs1057519124
SNPdbers1057519124
MSV3drs1057519124
GWAS Ctlgrs1057519124
Max Magnitude0
ClinVar
Risk rs1057519124(A;A)
Alt rs1057519124(A;A)
Reference Rs1057519124(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62073758C>T
CLNSRC
CLNACC RCV000416126.1,