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rs199473664

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473664(A;A)
Make rs199473664(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974833
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473664
ebirs199473664
HLIrs199473664
Exacrs199473664
Varsomers199473664
Maprs199473664
PheGenIrs199473664
hapmaprs199473664
1000 genomesrs199473664
hgdprs199473664
ensemblrs199473664
gopubmedrs199473664
geneviewrs199473664
scholarrs199473664
googlers199473664
pharmgkbrs199473664
gwascentralrs199473664
openSNPrs199473664
23andMers199473664
23andMe allrs199473664
SNP Nexus

SNPshotrs199473664
SNPdbers199473664
MSV3drs199473664
GWAS Ctlgrs199473664
Max Magnitude0
ClinVar
Risk rs199473664(A;A)
Alt rs199473664(A;A)
Reference rs199473664(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.150671921C>T
CLNSRC ClinVar
CLNACC RCV000058016.2,