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rs199473517

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473517(G;T)
Make rs199473517(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951704
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473517
ClinGenrs199473517
ebirs199473517
HLIrs199473517
Exacrs199473517
Varsomers199473517
Maprs199473517
PheGenIrs199473517
hapmaprs199473517
1000 genomesrs199473517
hgdprs199473517
ensemblrs199473517
gopubmedrs199473517
geneviewrs199473517
scholarrs199473517
googlers199473517
pharmgkbrs199473517
gwascentralrs199473517
openSNPrs199473517
23andMers199473517
23andMe allrs199473517
SNP Nexus

SNPshotrs199473517
SNPdbers199473517
MSV3drs199473517
GWAS Ctlgrs199473517
Max Magnitude0
ClinVar
Risk rs199473517(C;C) rs199473517(T;T)
Alt rs199473517(C;C) rs199473517(T;T)
Reference Rs199473517(G;G)
Significance Untested
Disease Congenital long QT syndrome not specified
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome not specified
Reversed 1
HGVS NC_000007.13:g.150648792C>A; NC_000007.13:g.150648792C>G
CLNSRC ClinVar
CLNACC RCV000057945.3, RCV000181808.2,