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rs199473375

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473375(G;G)
Make rs199473375(G;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175407
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473375
ebirs199473375
HLIrs199473375
Exacrs199473375
Varsomers199473375
Maprs199473375
PheGenIrs199473375
hapmaprs199473375
1000 genomesrs199473375
hgdprs199473375
ensemblrs199473375
gopubmedrs199473375
geneviewrs199473375
scholarrs199473375
googlers199473375
pharmgkbrs199473375
gwascentralrs199473375
openSNPrs199473375
23andMers199473375
23andMe allrs199473375
SNP Nexus

SNPshotrs199473375
SNPdbers199473375
MSV3drs199473375
GWAS Ctlgrs199473375
Max Magnitude0
ClinVar
Risk rs199473375(G;G)
Alt rs199473375(G;G)
Reference rs199473375(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.68171548T>G
CLNSRC ClinVar
CLNACC RCV000058309.2,