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rs199473658

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473658(A;A)
Make rs199473658(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175960
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473658
ebirs199473658
HLIrs199473658
Exacrs199473658
Varsomers199473658
Maprs199473658
PheGenIrs199473658
hapmaprs199473658
1000 genomesrs199473658
hgdprs199473658
ensemblrs199473658
gopubmedrs199473658
geneviewrs199473658
scholarrs199473658
googlers199473658
pharmgkbrs199473658
gwascentralrs199473658
openSNPrs199473658
23andMers199473658
23andMe allrs199473658
SNP Nexus

SNPshotrs199473658
SNPdbers199473658
MSV3drs199473658
GWAS Ctlgrs199473658
Max Magnitude0
ClinVar
Risk rs199473658(A;A)
Alt rs199473658(A;A)
Reference rs199473658(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.68172101G>A
CLNSRC ClinVar
CLNACC RCV000058337.2,