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rs199473654

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473654(A;A)
Make rs199473654(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position70175475
GeneKCNJ2
is asnp
is mentioned by
dbSNPrs199473654
ebirs199473654
HLIrs199473654
Exacrs199473654
Varsomers199473654
Maprs199473654
PheGenIrs199473654
hapmaprs199473654
1000 genomesrs199473654
hgdprs199473654
ensemblrs199473654
gopubmedrs199473654
geneviewrs199473654
scholarrs199473654
googlers199473654
pharmgkbrs199473654
gwascentralrs199473654
openSNPrs199473654
23andMers199473654
23andMe allrs199473654
SNP Nexus

SNPshotrs199473654
SNPdbers199473654
MSV3drs199473654
GWAS Ctlgrs199473654
Max Magnitude0
ClinVar
Risk rs199473654(A;A)
Alt rs199473654(A;A)
Reference rs199473654(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.68171616G>A
CLNSRC ClinVar
CLNACC RCV000058314.2,