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rs3176124

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3176124(C;T)
Make rs3176124(T;T)
ReferenceGRCh38 38.1/142
Chromosome20
Position23046308
GeneTHBD
is asnp
is mentioned by
dbSNPrs3176124
ClinGenrs3176124
ebirs3176124
HLIrs3176124
Exacrs3176124
Varsomers3176124
Maprs3176124
PheGenIrs3176124
Biobankrs3176124
1000 genomesrs3176124
hgdprs3176124
ensemblrs3176124
gopubmedrs3176124
geneviewrs3176124
scholarrs3176124
googlers3176124
pharmgkbrs3176124
gwascentralrs3176124
openSNPrs3176124
23andMers3176124
23andMe allrs3176124
SNP Nexus

SNPshotrs3176124
SNPdbers3176124
MSV3drs3176124
GWAS Ctlgrs3176124
Max Magnitude0

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


ClinVar
Risk rs3176124(T;T)
Alt rs3176124(T;T)
Reference Rs3176124(C;C)
Significance Probable-non-pathogenic
Disease Atypical hemolytic uremic syndrome
Variation info
Gene THBD
CLNDBN Atypical hemolytic uremic syndrome
Reversed 1
HGVS NC_000020.10:g.23026945G>A
CLNSRC
CLNACC RCV000400358.1,