rs5368

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(C;T)
(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

169727805

Gene

SELE

is a	snp
is	mentioned by
dbSNP	rs5368
dbSNP (classic)	rs5368
ClinGen	rs5368
ebi	rs5368
HLI	rs5368
Exac	rs5368
Gnomad	rs5368
Varsome	rs5368
LitVar	rs5368
Map	rs5368
PheGenI	rs5368
Biobank	rs5368
1000 genomes	rs5368
hgdp	rs5368
ensembl	rs5368
geneview	rs5368
scholar	rs5368
google	rs5368
pharmgkb	rs5368
gwascentral	rs5368
openSNP	rs5368
23andMe	rs5368
SNPshot	rs5368
SNPdbe	rs5368
MSV3d	rs5368
GWAS Ctlg	rs5368

GMAF

0.1616

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 19240957] Candidate gene analysis of selectin cluster in patients with multiple sclerosis

OMIM	131210
Desc
Variant	0001
Related	also

ClinVar
Risk	Rs5368(T;T)
Alt	Rs5368(T;T)
Reference	Rs5368(C;C)
Significance	Unknown
Disease	IgA nephropathy
Variation	info
Gene	SELE
CLNDBN	IgA nephropathy, susceptibility to
Reversed	1
HGVS	NC_000001.10:g.169696946G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018147.2,

[PMID 20388367] [Polymorphisms of vascular diseases-related genes in Guangzhou Biobank Cohort Study].

[PMID 23190470 ] Association of SELE genotypes/haplotypes with sE-selectin levels in Taiwanese individuals: interactive effect of MMP9 level

[PMID 26194693] Polymorphisms in host genes encoding NOSII, C-reactive protein, and adhesion molecules thrombospondin and E-selectin are risk factors for Plasmodium falciparum malaria in India