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rs786205426

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205426(C;T)
Make rs786205426(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position33408527
GeneSNTA1
is asnp
is mentioned by
dbSNPrs786205426
ebirs786205426
HLIrs786205426
Exacrs786205426
Varsomers786205426
Maprs786205426
PheGenIrs786205426
hapmaprs786205426
1000 genomesrs786205426
hgdprs786205426
ensemblrs786205426
gopubmedrs786205426
geneviewrs786205426
scholarrs786205426
googlers786205426
pharmgkbrs786205426
gwascentralrs786205426
openSNPrs786205426
23andMers786205426
23andMe allrs786205426
SNP Nexus

SNPshotrs786205426
SNPdbers786205426
MSV3drs786205426
GWAS Ctlgrs786205426
Max Magnitude0
ClinVar
Risk rs786205426(T;T)
Alt rs786205426(T;T)
Reference rs786205426(C;C)
Significance Probable-Pathogenic
Disease not provided Long QT syndrome
Variation info
Gene SNTA1
CLNDBN not provided Long QT syndrome
Reversed 1
HGVS NC_000020.10:g.31996333G>A
CLNSRC
CLNACC RCV000171705.1, RCV000190224.1,