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rs3213787

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs3213787(A;G)
Make rs3213787(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position45419685
GeneSRBD1
is asnp
is mentioned by
dbSNPrs3213787
ebirs3213787
HLIrs3213787
Exacrs3213787
Varsomers3213787
Maprs3213787
PheGenIrs3213787
hapmaprs3213787
1000 genomesrs3213787
hgdprs3213787
ensemblrs3213787
gopubmedrs3213787
geneviewrs3213787
scholarrs3213787
googlers3213787
pharmgkbrs3213787
gwascentralrs3213787
openSNPrs3213787
23andMers3213787
23andMe allrs3213787
SNP Nexus

SNPshotrs3213787
SNPdbers3213787
MSV3drs3213787
GWAS Ctlgrs3213787
GMAF0.07254
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20363506]
Trait Glaucoma
Title Genome-wide Association Study of Normal Tension Glaucoma: Common Variants in SRBD1 and ELOVL5 Contribute to Disease Susceptibility
Risk Allele A
P-val 3E-9
Odds Ratio 2.80 [1.96-3.99]


[PMID 22792221OA-icon.png] Common Variants on Chromosome 9p21 Are Associated with Normal Tension Glaucoma

[PMID 21508110] Association between SRBD1 and ELOVL5 gene polymorphisms and primary open-angle glaucoma.