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rs1057518492

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518492(A;A)
Make rs1057518492(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position63414088
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1057518492
dbSNP (old)rs1057518492
ClinGenrs1057518492
ebirs1057518492
HLIrs1057518492
Exacrs1057518492
Gnomadrs1057518492
Varsomers1057518492
LitVarrs1057518492
Maprs1057518492
PheGenIrs1057518492
Biobankrs1057518492
1000 genomesrs1057518492
hgdprs1057518492
ensemblrs1057518492
gopubmedrs1057518492
geneviewrs1057518492
scholarrs1057518492
googlers1057518492
pharmgkbrs1057518492
gwascentralrs1057518492
openSNPrs1057518492
23andMers1057518492
23andMe allrs1057518492
SNPshotrs1057518492
SNPdbers1057518492
MSV3drs1057518492
GWAS Ctlgrs1057518492
Max Magnitude0
ClinVar
Risk rs1057518492(A;A)
Alt rs1057518492(A;A)
Reference Rs1057518492(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62045441C>T
CLNSRC
CLNACC RCV000412766.1,