rs3176124

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs3176124(C;T)

Make rs3176124(T;T)

Reference

GRCh38 38.1/142

Chromosome

20

Position

23046308

Gene

THBD

is a	snp
is	mentioned by
dbSNP	rs3176124
dbSNP (classic)	rs3176124
ClinGen	rs3176124
ebi	rs3176124
HLI	rs3176124
Exac	rs3176124
Gnomad	rs3176124
Varsome	rs3176124
LitVar	rs3176124
Map	rs3176124
PheGenI	rs3176124
Biobank	rs3176124
1000 genomes	rs3176124
hgdp	rs3176124
ensembl	rs3176124
geneview	rs3176124
scholar	rs3176124
google	rs3176124
pharmgkb	rs3176124
gwascentral	rs3176124
openSNP	rs3176124
23andMe	rs3176124
SNPshot	rs3176124
SNPdbe	rs3176124
MSV3d	rs3176124
GWAS Ctlg	rs3176124

Max Magnitude

0

[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,