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rs16872571

From SNPedia

Orientationplus
Stabilizedplus
Make rs16872571(C;C)
Make rs16872571(C;T)
Make rs16872571(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position10725229
is asnp
is mentioned by
dbSNPrs16872571
ebirs16872571
HLIrs16872571
Exacrs16872571
Varsomers16872571
Maprs16872571
PheGenIrs16872571
hapmaprs16872571
1000 genomesrs16872571
hgdprs16872571
ensemblrs16872571
gopubmedrs16872571
geneviewrs16872571
scholarrs16872571
googlers16872571
pharmgkbrs16872571
gwascentralrs16872571
openSNPrs16872571
23andMers16872571
23andMe allrs16872571
SNP Nexus

SNPshotrs16872571
SNPdbers16872571
MSV3drs16872571
GWAS Ctlgrs16872571
GMAF0.2769
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22561518OA-icon.png]
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