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rs1057520623

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520623(A;A)
Make rs1057520623(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position2572908
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs1057520623
dbSNP (old)rs1057520623
ClinGenrs1057520623
ebirs1057520623
HLIrs1057520623
Exacrs1057520623
Gnomadrs1057520623
Varsomers1057520623
Maprs1057520623
PheGenIrs1057520623
Biobankrs1057520623
1000 genomesrs1057520623
hgdprs1057520623
ensemblrs1057520623
gopubmedrs1057520623
geneviewrs1057520623
scholarrs1057520623
googlers1057520623
pharmgkbrs1057520623
gwascentralrs1057520623
openSNPrs1057520623
23andMers1057520623
23andMe allrs1057520623
SNPshotrs1057520623
SNPdbers1057520623
MSV3drs1057520623
GWAS Ctlgrs1057520623
Max Magnitude0
ClinVar
Risk rs1057520623(A;A)
Alt rs1057520623(A;A)
Reference Rs1057520623(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2594138C>A
CLNSRC
CLNACC RCV000433921.1,