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rs1057518068

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518068(C;C)
Make rs1057518068(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position63442479
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1057518068
dbSNP (old)rs1057518068
ClinGenrs1057518068
ebirs1057518068
HLIrs1057518068
Exacrs1057518068
Gnomadrs1057518068
Varsomers1057518068
Maprs1057518068
PheGenIrs1057518068
Biobankrs1057518068
1000 genomesrs1057518068
hgdprs1057518068
ensemblrs1057518068
gopubmedrs1057518068
geneviewrs1057518068
scholarrs1057518068
googlers1057518068
pharmgkbrs1057518068
gwascentralrs1057518068
openSNPrs1057518068
23andMers1057518068
23andMe allrs1057518068
SNPshotrs1057518068
SNPdbers1057518068
MSV3drs1057518068
GWAS Ctlgrs1057518068
Max Magnitude0
ClinVar
Risk rs1057518068(C;C)
Alt rs1057518068(C;C)
Reference Rs1057518068(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62073832A>G
CLNSRC
CLNACC RCV000414529.1,