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rs796052196

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052196(A;A)
Make rs796052196(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974709
GeneKCNH2
is asnp
is mentioned by
dbSNPrs796052196
ebirs796052196
HLIrs796052196
Exacrs796052196
Varsomers796052196
Maprs796052196
PheGenIrs796052196
hapmaprs796052196
1000 genomesrs796052196
hgdprs796052196
ensemblrs796052196
gopubmedrs796052196
geneviewrs796052196
scholarrs796052196
googlers796052196
pharmgkbrs796052196
gwascentralrs796052196
openSNPrs796052196
23andMers796052196
23andMe allrs796052196
SNP Nexus

SNPshotrs796052196
SNPdbers796052196
MSV3drs796052196
GWAS Ctlgrs796052196
Max Magnitude0
ClinVar
Risk rs796052196(A;A)
Alt rs796052196(A;A)
Reference rs796052196(T;T)
Significance Probable-Pathogenic
Disease Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150671797A>T
CLNSRC
CLNACC RCV000190216.1,