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rs199473346

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473346(A;A)
Make rs199473346(A;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position113363439
GeneANK2
is asnp
is mentioned by
dbSNPrs199473346
ebirs199473346
HLIrs199473346
Exacrs199473346
Varsomers199473346
Maprs199473346
PheGenIrs199473346
hapmaprs199473346
1000 genomesrs199473346
hgdprs199473346
ensemblrs199473346
gopubmedrs199473346
geneviewrs199473346
scholarrs199473346
googlers199473346
pharmgkbrs199473346
gwascentralrs199473346
openSNPrs199473346
23andMers199473346
23andMe allrs199473346
SNP Nexus

SNPshotrs199473346
SNPdbers199473346
MSV3drs199473346
GWAS Ctlgrs199473346
Max Magnitude0
ClinVar
Risk rs199473346(A;A)
Alt rs199473346(A;A)
Reference rs199473346(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene ANK2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000004.11:g.114284595T>A
CLNSRC Cardiovascular Biomedical Research Unit ClinVar
CLNACC RCV000058341.2,