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rs66785829

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs66785829(A;A)
Make rs66785829(A;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position113365051
GeneANK2
is asnp
is mentioned by
dbSNPrs66785829
ebirs66785829
HLIrs66785829
Exacrs66785829
Varsomers66785829
Maprs66785829
PheGenIrs66785829
hapmaprs66785829
1000 genomesrs66785829
hgdprs66785829
ensemblrs66785829
gopubmedrs66785829
geneviewrs66785829
scholarrs66785829
googlers66785829
pharmgkbrs66785829
gwascentralrs66785829
openSNPrs66785829
23andMers66785829
23andMe allrs66785829
SNP Nexus

SNPshotrs66785829
SNPdbers66785829
MSV3drs66785829
GWAS Ctlgrs66785829
Merged fromRs66785830
Max Magnitude0
ClinVar
Risk rs66785829(A;A)
Alt rs66785829(A;A)
Reference rs66785829(T;T)
Significance Pathogenic
Disease Arrhythmia Long QT syndrome Cardiac arrhythmia not specified
Variation info
Gene ANK2
CLNDBN Arrhythmia Long QT syndrome Cardiac arrhythmia not specified
Reversed 0
HGVS NC_000004.11:g.114286207T>A
CLNSRC Cardiovascular Biomedical Research Unit ClinVar GeneDx
CLNACC RCV000058344.2, RCV000168225.2, RCV000171748.3, RCV000211889.1,