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rs199473416

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473416(G;G)
Make rs199473416(G;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974822
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473416
ebirs199473416
HLIrs199473416
Exacrs199473416
Varsomers199473416
Maprs199473416
PheGenIrs199473416
hapmaprs199473416
1000 genomesrs199473416
hgdprs199473416
ensemblrs199473416
gopubmedrs199473416
geneviewrs199473416
scholarrs199473416
googlers199473416
pharmgkbrs199473416
gwascentralrs199473416
openSNPrs199473416
23andMers199473416
23andMe allrs199473416
SNP Nexus

SNPshotrs199473416
SNPdbers199473416
MSV3drs199473416
GWAS Ctlgrs199473416
Max Magnitude0
ClinVar
Risk rs199473416(G;G)
Alt rs199473416(G;G)
Reference rs199473416(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150671910A>C
CLNSRC ClinVar
CLNACC RCV000058071.2,