rs80358315

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs80358315(C;G)

Make rs80358315(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

68410124

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs80358315
dbSNP (classic)	rs80358315
ClinGen	rs80358315
ebi	rs80358315
HLI	rs80358315
Exac	rs80358315
Gnomad	rs80358315
Varsome	rs80358315
LitVar	rs80358315
Map	rs80358315
PheGenI	rs80358315
Biobank	rs80358315
1000 genomes	rs80358315
hgdp	rs80358315
ensembl	rs80358315
geneview	rs80358315
scholar	rs80358315
google	rs80358315
pharmgkb	rs80358315
gwascentral	rs80358315
openSNP	rs80358315
23andMe	rs80358315
SNPshot	rs80358315
SNPdbe	rs80358315
MSV3d	rs80358315
GWAS Ctlg	rs80358315

Max Magnitude

0

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 15346351] Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5.