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rs148654834

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148654834(C;C)
Make rs148654834(C;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position113369711
GeneANK2
is asnp
is mentioned by
dbSNPrs148654834
ebirs148654834
HLIrs148654834
Exacrs148654834
Varsomers148654834
Maprs148654834
PheGenIrs148654834
hapmaprs148654834
1000 genomesrs148654834
hgdprs148654834
ensemblrs148654834
gopubmedrs148654834
geneviewrs148654834
scholarrs148654834
googlers148654834
pharmgkbrs148654834
gwascentralrs148654834
openSNPrs148654834
23andMers148654834
23andMe allrs148654834
SNP Nexus

SNPshotrs148654834
SNPdbers148654834
MSV3drs148654834
GWAS Ctlgrs148654834
Max Magnitude0
ClinVar
Risk rs148654834(C;C)
Alt rs148654834(C;C)
Reference rs148654834(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene ANK2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000004.11:g.114290867G>C
CLNSRC Cardiovascular Biomedical Research Unit ClinVar
CLNACC RCV000058348.2,