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rs3176123

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3176123(A;C)
Make rs3176123(C;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position23046776
GeneTHBD
is asnp
is mentioned by
dbSNPrs3176123
dbSNP (classic)rs3176123
ClinGenrs3176123
ebirs3176123
HLIrs3176123
Exacrs3176123
Gnomadrs3176123
Varsomers3176123
LitVarrs3176123
Maprs3176123
PheGenIrs3176123
Biobankrs3176123
1000 genomesrs3176123
hgdprs3176123
ensemblrs3176123
geneviewrs3176123
scholarrs3176123
googlers3176123
pharmgkbrs3176123
gwascentralrs3176123
openSNPrs3176123
23andMers3176123
SNPshotrs3176123
SNPdbers3176123
MSV3drs3176123
GWAS Ctlgrs3176123
GMAF0.1685
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 21911804OA-icon.png] Thrombomodulin gene variants are associated with increased mortality after coronary artery bypass surgery in replicated analyses


[PMID 18035074OA-icon.png] Association of polymorphisms in platelet and hemostasis system genes with acute myocardial infarction.


[PMID 24602049] Association of gene polymorphisms with the risk of warfarin bleeding complications at therapeutic INR in patients with mechanical cardiac valves


[PMID 25225421] Single-Nucleotide Polymorphisms Within the Thrombomodulin Gene (THBD) Predict Mortality in Patients With Graft-Versus-Host Disease


ClinVar
Risk rs3176123(C;C)
Alt rs3176123(C;C)
Reference Rs3176123(A;A)
Significance Non-pathogenic
Disease Atypical hemolytic uremic syndrome
Variation info
Gene THBD
CLNDBN Atypical hemolytic uremic syndrome
Reversed 1
HGVS NC_000020.10:g.23027413T>G
CLNSRC
CLNACC RCV000367420.1,