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rs199473508

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473508(C;C)
Make rs199473508(C;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952697
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473508
ebirs199473508
HLIrs199473508
Exacrs199473508
Varsomers199473508
Maprs199473508
PheGenIrs199473508
hapmaprs199473508
1000 genomesrs199473508
hgdprs199473508
ensemblrs199473508
gopubmedrs199473508
geneviewrs199473508
scholarrs199473508
googlers199473508
pharmgkbrs199473508
gwascentralrs199473508
openSNPrs199473508
23andMers199473508
23andMe allrs199473508
SNP Nexus

SNPshotrs199473508
SNPdbers199473508
MSV3drs199473508
GWAS Ctlgrs199473508
Max Magnitude0
ClinVar
Risk rs199473508(C;C)
Alt rs199473508(C;C)
Reference rs199473508(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150649785C>G
CLNSRC ClinVar
CLNACC RCV000057888.2,