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rs199473370

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473370(A;G)
Make rs199473370(G;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175262
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473370
ebirs199473370
HLIrs199473370
Exacrs199473370
Varsomers199473370
Maprs199473370
PheGenIrs199473370
hapmaprs199473370
1000 genomesrs199473370
hgdprs199473370
ensemblrs199473370
gopubmedrs199473370
geneviewrs199473370
scholarrs199473370
googlers199473370
pharmgkbrs199473370
gwascentralrs199473370
openSNPrs199473370
23andMers199473370
23andMe allrs199473370
SNP Nexus

SNPshotrs199473370
SNPdbers199473370
MSV3drs199473370
GWAS Ctlgrs199473370
Max Magnitude0
ClinVar
Risk rs199473370(G;G)
Alt rs199473370(G;G)
Reference rs199473370(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNJ2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000017.10:g.68171403A>G
CLNSRC ClinVar
CLNACC RCV000058300.2,