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rs143228029

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs143228029(A;A)
Make rs143228029(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position113365050
GeneANK2
is asnp
is mentioned by
dbSNPrs143228029
ebirs143228029
HLIrs143228029
Exacrs143228029
Varsomers143228029
Maprs143228029
PheGenIrs143228029
hapmaprs143228029
1000 genomesrs143228029
hgdprs143228029
ensemblrs143228029
gopubmedrs143228029
geneviewrs143228029
scholarrs143228029
googlers143228029
pharmgkbrs143228029
gwascentralrs143228029
openSNPrs143228029
23andMers143228029
23andMe allrs143228029
SNP Nexus

SNPshotrs143228029
SNPdbers143228029
MSV3drs143228029
GWAS Ctlgrs143228029
Max Magnitude0
ClinVar
Risk rs143228029(A;A)
Alt rs143228029(A;A)
Reference rs143228029(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.114286206G>A
CLNSRC Cardiovascular Biomedical Research Unit ClinVar
CLNACC RCV000058343.2,