rs17568

Orientation

minus

Stabilized

minus

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

Make rs17568(A;A)

Make rs17568(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

1212042

Gene

TNFRSF4

is a	snp
is	mentioned by
dbSNP	rs17568
dbSNP (classic)	rs17568
ClinGen	rs17568
ebi	rs17568
HLI	rs17568
Exac	rs17568
Gnomad	rs17568
Varsome	rs17568
LitVar	rs17568
Map	rs17568
PheGenI	rs17568
Biobank	rs17568
1000 genomes	rs17568
hgdp	rs17568
ensembl	rs17568
geneview	rs17568
scholar	rs17568
google	rs17568
pharmgkb	rs17568
gwascentral	rs17568
openSNP	rs17568
23andMe	rs17568
SNPshot	rs17568
SNPdbe	rs17568
MSV3d	rs17568
GWAS Ctlg	rs17568

GMAF

0.4559

Max Magnitude

0

[PMID 24595151] Absence of association between atherosclerotic cerebral infarction and TNFSF4/TNFRSF4 single nucleotide polymorphisms rs1234313, rs1234314 and rs17568 in a Chinese population [PMID 18798503] [Correlation of OX40 gene rs17568A/G polymorphism with acute coronary syndrome in Chinese Han population].

[PMID 18987746] Association of interacting genes in the toll-like receptor signaling pathway and the antibody response to pertussis vaccination.

[PMID 21476935] Association of OX40 and OX40L gene polymorphisms with acute coronary syndrome in a Han Chinese population.

[PMID 23216302] Genetic variation in the OX40L/OX40 system and plasma lipid and lipoprotein levels in a Chinese hypertriglyceridemic population. [PMID 26755473] Lack of Association Between rs17568 Polymorphism in OX40 Gene and Myocardial Infarction, Southern of Iran.

ClinVar
Risk	rs17568(A;A)
Alt	rs17568(A;A)
Reference	Rs17568(G;G)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	TNFRSF4
CLNDBN	not specified
Reversed	1
HGVS	NC_000001.10:g.1147422C>T
CLNSRC
CLNACC	RCV000455786.1,

[PMID 30923998] Association of OX40 gene polymorphisms (rs17568G/A and rs229811A/C) with head and neck squamous cell carcinoma.