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rs80358315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80358315(C;G)
Make rs80358315(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position68410124
GeneLRP5
is asnp
is mentioned by
dbSNPrs80358315
ebirs80358315
HLIrs80358315
Exacrs80358315
Varsomers80358315
Maprs80358315
PheGenIrs80358315
hapmaprs80358315
1000 genomesrs80358315
hgdprs80358315
ensemblrs80358315
gopubmedrs80358315
geneviewrs80358315
scholarrs80358315
googlers80358315
pharmgkbrs80358315
gwascentralrs80358315
openSNPrs80358315
23andMers80358315
23andMe allrs80358315
SNP Nexus

SNPshotrs80358315
SNPdbers80358315
MSV3drs80358315
GWAS Ctlgrs80358315
Max Magnitude0
ClinVar
Risk rs80358315(G;G)
Alt rs80358315(G;G)
Reference rs80358315(C;C)
Significance Untested
Disease
Variation info
Gene LRP5
CLNDBN
Reversed 0
HGVS NC_000011.9:g.68177592C>G
CLNSRC
CLNACC


[PMID 15346351OA-icon.png] Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5.