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rs1060500628

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500628(G;T)
Make rs1060500628(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position2572062
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs1060500628
dbSNP (old)rs1060500628
ClinGenrs1060500628
ebirs1060500628
HLIrs1060500628
Exacrs1060500628
Gnomadrs1060500628
Varsomers1060500628
Maprs1060500628
PheGenIrs1060500628
Biobankrs1060500628
1000 genomesrs1060500628
hgdprs1060500628
ensemblrs1060500628
gopubmedrs1060500628
geneviewrs1060500628
scholarrs1060500628
googlers1060500628
pharmgkbrs1060500628
gwascentralrs1060500628
openSNPrs1060500628
23andMers1060500628
23andMe allrs1060500628
SNPshotrs1060500628
SNPdbers1060500628
MSV3drs1060500628
GWAS Ctlgrs1060500628
Max Magnitude0
ClinVar
Risk rs1060500628(T;T)
Alt rs1060500628(T;T)
Reference Rs1060500628(G;G)
Significance Pathogenic
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2593292G>T
CLNSRC
CLNACC RCV000459171.1,