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rs1057524599

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524599(A;G)
Make rs1057524599(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position63444718
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1057524599
dbSNP (old)rs1057524599
ClinGenrs1057524599
ebirs1057524599
HLIrs1057524599
Exacrs1057524599
Gnomadrs1057524599
Varsomers1057524599
Maprs1057524599
PheGenIrs1057524599
Biobankrs1057524599
1000 genomesrs1057524599
hgdprs1057524599
ensemblrs1057524599
gopubmedrs1057524599
geneviewrs1057524599
scholarrs1057524599
googlers1057524599
pharmgkbrs1057524599
gwascentralrs1057524599
openSNPrs1057524599
23andMers1057524599
23andMe allrs1057524599
SNPshotrs1057524599
SNPdbers1057524599
MSV3drs1057524599
GWAS Ctlgrs1057524599
Max Magnitude0
ClinVar
Risk rs1057524599(G;G)
Alt rs1057524599(G;G)
Reference Rs1057524599(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62076071T>C
CLNSRC
CLNACC RCV000434548.1,