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rs121912509

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912509(A;A)
Make rs121912509(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position150947477
GeneKCNH2
is asnp
is mentioned by
dbSNPrs121912509
ebirs121912509
HLIrs121912509
Exacrs121912509
Varsomers121912509
Maprs121912509
PheGenIrs121912509
hapmaprs121912509
1000 genomesrs121912509
hgdprs121912509
ensemblrs121912509
gopubmedrs121912509
geneviewrs121912509
scholarrs121912509
googlers121912509
pharmgkbrs121912509
gwascentralrs121912509
openSNPrs121912509
23andMers121912509
23andMe allrs121912509
SNP Nexus

SNPshotrs121912509
SNPdbers121912509
MSV3drs121912509
GWAS Ctlgrs121912509
Max Magnitude0
OMIM152427
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121912509(A;A)
Alt rs121912509(A;A)
Reference rs121912509(G;G)
Significance Pathogenic
Disease Long QT syndrome 2 not provided
Variation info
Gene KCNH2
CLNDBN Long QT syndrome 2 not provided
Reversed 1
HGVS NC_000007.13:g.150644565C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015512.25, RCV000181905.1,