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rs199473643

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473643(A;A)
Make rs199473643(A;C)
ReferenceGRCh38 38.1/142
Chromosome4
Position113369726
GeneANK2
is asnp
is mentioned by
dbSNPrs199473643
ebirs199473643
HLIrs199473643
Exacrs199473643
Varsomers199473643
Maprs199473643
PheGenIrs199473643
hapmaprs199473643
1000 genomesrs199473643
hgdprs199473643
ensemblrs199473643
gopubmedrs199473643
geneviewrs199473643
scholarrs199473643
googlers199473643
pharmgkbrs199473643
gwascentralrs199473643
openSNPrs199473643
23andMers199473643
23andMe allrs199473643
SNP Nexus

SNPshotrs199473643
SNPdbers199473643
MSV3drs199473643
GWAS Ctlgrs199473643
Max Magnitude0
ClinVar
Risk rs199473643(A;A)
Alt rs199473643(A;A)
Reference rs199473643(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene ANK2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000004.11:g.114290882C>A
CLNSRC Cardiovascular Biomedical Research Unit ClinVar
CLNACC RCV000058349.2,