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rs199473380

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473380(G;T)
Make rs199473380(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175500
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473380
ebirs199473380
HLIrs199473380
Exacrs199473380
Varsomers199473380
Maprs199473380
PheGenIrs199473380
hapmaprs199473380
1000 genomesrs199473380
hgdprs199473380
ensemblrs199473380
gopubmedrs199473380
geneviewrs199473380
scholarrs199473380
googlers199473380
pharmgkbrs199473380
gwascentralrs199473380
openSNPrs199473380
23andMers199473380
23andMe allrs199473380
SNP Nexus

SNPshotrs199473380
SNPdbers199473380
MSV3drs199473380
GWAS Ctlgrs199473380
Max Magnitude0
ClinVar
Risk rs199473380(T;T)
Alt rs199473380(T;T)
Reference rs199473380(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNJ2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000017.10:g.68171641G>T
CLNSRC ClinVar
CLNACC RCV000058317.2,