Have questions? Visit https://www.reddit.com/r/SNPedia

rs80358309

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358309(A;A)
Make rs80358309(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position68390032
GeneLRP5
is asnp
is mentioned by
dbSNPrs80358309
ebirs80358309
HLIrs80358309
Exacrs80358309
Varsomers80358309
Maprs80358309
PheGenIrs80358309
hapmaprs80358309
1000 genomesrs80358309
hgdprs80358309
ensemblrs80358309
gopubmedrs80358309
geneviewrs80358309
scholarrs80358309
googlers80358309
pharmgkbrs80358309
gwascentralrs80358309
openSNPrs80358309
23andMers80358309
23andMe allrs80358309
SNP Nexus

SNPshotrs80358309
SNPdbers80358309
MSV3drs80358309
GWAS Ctlgrs80358309
Max Magnitude0
ClinVar
Risk rs80358309(A;A)
Alt rs80358309(A;A)
Reference rs80358309(G;G)
Significance Pathogenic
Disease Exudative vitreoretinopathy 4
Variation info
Gene LRP5
CLNDBN Exudative vitreoretinopathy 4
Reversed 0
HGVS NC_000011.9:g.68157500G>A
CLNSRC
CLNACC


[PMID 15981244] Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes.