rs3176134

Orientation

minus

Stabilized

minus

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

Make rs3176134(A;A)

Make rs3176134(A;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

23047500

Gene

THBD

is a	snp
is	mentioned by
dbSNP	rs3176134
dbSNP (classic)	rs3176134
ClinGen	rs3176134
ebi	rs3176134
HLI	rs3176134
Exac	rs3176134
Gnomad	rs3176134
Varsome	rs3176134
LitVar	rs3176134
Map	rs3176134
PheGenI	rs3176134
Biobank	rs3176134
1000 genomes	rs3176134
hgdp	rs3176134
ensembl	rs3176134
geneview	rs3176134
scholar	rs3176134
google	rs3176134
pharmgkb	rs3176134
gwascentral	rs3176134
openSNP	rs3176134
23andMe	rs3176134
SNPshot	rs3176134
SNPdbe	rs3176134
MSV3d	rs3176134
GWAS Ctlg	rs3176134

Max Magnitude

0

?	(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,