Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473528

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473528(A;G)
Make rs199473528(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951481
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473528
dbSNP (old)rs199473528
ClinGenrs199473528
ebirs199473528
HLIrs199473528
Exacrs199473528
Gnomadrs199473528
Varsomers199473528
Maprs199473528
PheGenIrs199473528
Biobankrs199473528
1000 genomesrs199473528
hgdprs199473528
ensemblrs199473528
gopubmedrs199473528
geneviewrs199473528
scholarrs199473528
googlers199473528
pharmgkbrs199473528
gwascentralrs199473528
openSNPrs199473528
23andMers199473528
23andMe allrs199473528
SNP Nexus

SNPshotrs199473528
SNPdbers199473528
MSV3drs199473528
GWAS Ctlgrs199473528
Max Magnitude0
ClinVar
Risk rs199473528(G;G)
Alt rs199473528(G;G)
Reference Rs199473528(A;A)
Significance Untested
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648569T>C
CLNSRC UniProtKB (protein)
CLNACC RCV000058051.3,