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rs1015213

From SNPedia

Orientationplus
Stabilizedplus
Make rs1015213(C;C)
Make rs1015213(C;T)
Make rs1015213(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position51974981
is asnp
is mentioned by
dbSNPrs1015213
ebirs1015213
HLIrs1015213
Exacrs1015213
Varsomers1015213
Maprs1015213
PheGenIrs1015213
hapmaprs1015213
1000 genomesrs1015213
hgdprs1015213
ensemblrs1015213
gopubmedrs1015213
geneviewrs1015213
scholarrs1015213
googlers1015213
pharmgkbrs1015213
gwascentralrs1015213
openSNPrs1015213
23andMers1015213
23andMe allrs1015213
SNP Nexus

SNPshotrs1015213
SNPdbers1015213
MSV3drs1015213
GWAS Ctlgrs1015213
GMAF0.1249
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22922875OA-icon.png]
Trait Glaucoma (primary open-angle)
Title Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma.
Risk Allele A
P-val 3E-9
Odds Ratio 1.50 [NR]


[PMID 23847314OA-icon.png] Association study in a South Indian population supports rs1015213 as a risk factor for primary angle closure


[PMID 23505305OA-icon.png] Genotype-phenotype analysis of SNPs associated with primary angle closure glaucoma (rs1015213, rs3753841 and rs11024102) and ocular biometry in the EPIC-Norfolk Eye Study.


[PMID 26268645] [Statistical model analysis of primary angle closure glaucoma associated genes and SNP]