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rs199473656

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473656(C;C)
Make rs199473656(C;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175689
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473656
ebirs199473656
HLIrs199473656
Exacrs199473656
Varsomers199473656
Maprs199473656
PheGenIrs199473656
hapmaprs199473656
1000 genomesrs199473656
hgdprs199473656
ensemblrs199473656
gopubmedrs199473656
geneviewrs199473656
scholarrs199473656
googlers199473656
pharmgkbrs199473656
gwascentralrs199473656
openSNPrs199473656
23andMers199473656
23andMe allrs199473656
SNP Nexus

SNPshotrs199473656
SNPdbers199473656
MSV3drs199473656
GWAS Ctlgrs199473656
Max Magnitude0
ClinVar
Risk rs199473656(C;C)
Alt rs199473656(C;C)
Reference rs199473656(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNJ2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000017.10:g.68171830T>C
CLNSRC ClinVar
CLNACC RCV000058325.2,