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rs56157422

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs56157422(C;C)
Make rs56157422(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position33412714
GeneSNTA1
is asnp
is mentioned by
dbSNPrs56157422
ebirs56157422
HLIrs56157422
Exacrs56157422
Varsomers56157422
Maprs56157422
PheGenIrs56157422
hapmaprs56157422
1000 genomesrs56157422
hgdprs56157422
ensemblrs56157422
gopubmedrs56157422
geneviewrs56157422
scholarrs56157422
googlers56157422
pharmgkbrs56157422
gwascentralrs56157422
openSNPrs56157422
23andMers56157422
23andMe allrs56157422
SNP Nexus

SNPshotrs56157422
SNPdbers56157422
MSV3drs56157422
GWAS Ctlgrs56157422
Max Magnitude0
ClinVar
Risk rs56157422(A,C;A,C)
Alt rs56157422(A,C;A,C)
Reference rs56157422(G;G)
Significance Pathogenic
Disease Long QT syndrome Long QT syndrome 12
Variation info
Gene SNTA1
CLNDBN Long QT syndrome Long QT syndrome 12
Reversed 0
HGVS NC_000020.10:g.32000520G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000171774.1, RCV000191018.2,