rs3176126

Orientation

minus

Stabilized

minus

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

Make rs3176126(C;T)

Make rs3176126(T;T)

Reference

GRCh38 38.1/142

Chromosome

20

Position

23045634

Gene

THBD

is a	snp
is	mentioned by
dbSNP	rs3176126
dbSNP (classic)	rs3176126
ClinGen	rs3176126
ebi	rs3176126
HLI	rs3176126
Exac	rs3176126
Gnomad	rs3176126
Varsome	rs3176126
LitVar	rs3176126
Map	rs3176126
PheGenI	rs3176126
Biobank	rs3176126
1000 genomes	rs3176126
hgdp	rs3176126
ensembl	rs3176126
geneview	rs3176126
scholar	rs3176126
google	rs3176126
pharmgkb	rs3176126
gwascentral	rs3176126
openSNP	rs3176126
23andMe	rs3176126
SNPshot	rs3176126
SNPdbe	rs3176126
MSV3d	rs3176126
GWAS Ctlg	rs3176126

Max Magnitude

0

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

ClinVar
Risk	rs3176126(T;T)
Alt	rs3176126(T;T)
Reference	Rs3176126(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.23026271G>A
CLNSRC
CLNACC	RCV000279336.1,