rs16872571

Orientation

plus

Stabilized

plus

Make rs16872571(C;C)

Make rs16872571(C;T)

Make rs16872571(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

10725229

Gene

CLNK

is a	snp
is	mentioned by
dbSNP	rs16872571
dbSNP (classic)	rs16872571
ClinGen	rs16872571
ebi	rs16872571
HLI	rs16872571
Exac	rs16872571
Gnomad	rs16872571
Varsome	rs16872571
LitVar	rs16872571
Map	rs16872571
PheGenI	rs16872571
Biobank	rs16872571
1000 genomes	rs16872571
hgdp	rs16872571
ensembl	rs16872571
geneview	rs16872571
scholar	rs16872571
google	rs16872571
pharmgkb	rs16872571
gwascentral	rs16872571
openSNP	rs16872571
23andMe	rs16872571
SNPshot	rs16872571
SNPdbe	rs16872571
MSV3d	rs16872571
GWAS Ctlg	rs16872571

GMAF

0.2769

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 22561518]
Trait
Title	Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.
Risk Allele	C
P-val	2E-8
Odds Ratio	1.2100 None

GWAS snp
PMID	[PMID 23049088]
Trait	Myopia (pathological)
Title	A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
Risk Allele
P-val	2E-10
Odds Ratio	NR NR