rs13208776

plus

Geno	Mag	Summary
(A;A)		normal
(A;G)		normal
(G;G)		higher risk for generalized vitiligo

Reference

GRCh38 38.1/141

Chromosome

6

Position

168540944

Gene

SMOC2

is a	snp
is	mentioned by
dbSNP	rs13208776
dbSNP (classic)	rs13208776
ClinGen	rs13208776
ebi	rs13208776
HLI	rs13208776
Exac	rs13208776
Gnomad	rs13208776
Varsome	rs13208776
LitVar	rs13208776
Map	rs13208776
PheGenI	rs13208776
Biobank	rs13208776
1000 genomes	rs13208776
hgdp	rs13208776
ensembl	rs13208776
geneview	rs13208776
scholar	rs13208776
google	rs13208776
pharmgkb	rs13208776
gwascentral	rs13208776
openSNP	rs13208776
23andMe	rs13208776
SNPshot	rs13208776
SNPdbe	rs13208776
MSV3d	rs13208776
GWAS Ctlg	rs13208776

GMAF

0.1561

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

rs13208776 is a SNP in the SPARC related modular calcium binding 2 SMOC2 gene.

A genome-wide association study (GWAS) of generalized vitiligo in 32 distantly related affected patients from a remote Romanian village identified rs13208776 as highly associated with the disorder, at an odds ratio of 7.445 (CI: 3.5-15.3, p=8x10e-8) and a population attributable risk of 28.[PMID 19890347 ]

[PMID 20965805] SMOC2 gene variant and the risk of vitiligo in Jordanian Arabs

[PMID 23463390] Variants in PTPN22 and SMOC2 genes and the risk of thyroid disease in the Jordanian Arab population.