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rs45570339

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45570339(C;G)
Make rs45570339(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position113363442
GeneANK2
is asnp
is mentioned by
dbSNPrs45570339
ebirs45570339
HLIrs45570339
Exacrs45570339
Varsomers45570339
Maprs45570339
PheGenIrs45570339
hapmaprs45570339
1000 genomesrs45570339
hgdprs45570339
ensemblrs45570339
gopubmedrs45570339
geneviewrs45570339
scholarrs45570339
googlers45570339
pharmgkbrs45570339
gwascentralrs45570339
openSNPrs45570339
23andMers45570339
23andMe allrs45570339
SNP Nexus

SNPshotrs45570339
SNPdbers45570339
MSV3drs45570339
GWAS Ctlgrs45570339
Max Magnitude0
ClinVar
Risk rs45570339(G;G)
Alt rs45570339(G;G)
Reference rs45570339(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome not specified Long QT syndrome
Variation info
Gene ANK2
CLNDBN Congenital long QT syndrome not specified Long QT syndrome
Reversed 0
HGVS NC_000004.11:g.114284598C>G
CLNSRC Cardiovascular Biomedical Research Unit ClinVar
CLNACC RCV000058342.2, RCV000170658.3, RCV000171796.2,