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rs3176134

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3176134(A;A)
Make rs3176134(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position23047500
GeneTHBD
is asnp
is mentioned by
dbSNPrs3176134
dbSNP (old)rs3176134
ClinGenrs3176134
ebirs3176134
HLIrs3176134
Exacrs3176134
Gnomadrs3176134
Varsomers3176134
Maprs3176134
PheGenIrs3176134
Biobankrs3176134
1000 genomesrs3176134
hgdprs3176134
ensemblrs3176134
gopubmedrs3176134
geneviewrs3176134
scholarrs3176134
googlers3176134
pharmgkbrs3176134
gwascentralrs3176134
openSNPrs3176134
23andMers3176134
23andMe allrs3176134
SNP Nexus

SNPshotrs3176134
SNPdbers3176134
MSV3drs3176134
GWAS Ctlgrs3176134
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 25225421] Single-Nucleotide Polymorphisms Within the Thrombomodulin Gene (THBD) Predict Mortality in Patients With Graft-Versus-Host Disease


ClinVar
Risk rs3176134(A;A) rs3176134(T;T)
Alt rs3176134(A;A) rs3176134(T;T)
Reference Rs3176134(G;G)
Significance Non-pathogenic
Disease Atypical hemolytic uremic syndrome
Variation info
Gene THBD
CLNDBN Atypical hemolytic uremic syndrome
Reversed 1
HGVS NC_000020.10:g.23028137C>T
CLNSRC
CLNACC RCV000289808.1,