rs121908674

Orientation

plus

Stabilized

plus

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

Make rs121908674(C;G)

Make rs121908674(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

68410076

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs121908674
dbSNP (classic)	rs121908674
ClinGen	rs121908674
ebi	rs121908674
HLI	rs121908674
Exac	rs121908674
Gnomad	rs121908674
Varsome	rs121908674
LitVar	rs121908674
Map	rs121908674
PheGenI	rs121908674
Biobank	rs121908674
1000 genomes	rs121908674
hgdp	rs121908674
ensembl	rs121908674
geneview	rs121908674
scholar	rs121908674
google	rs121908674
pharmgkb	rs121908674
gwascentral	rs121908674
openSNP	rs121908674
23andMe	rs121908674
SNPshot	rs121908674
SNPdbe	rs121908674
MSV3d	rs121908674
GWAS Ctlg	rs121908674

Merged from

Rs28939708

Max Magnitude

0

OMIM	603506
Desc
Variant	0023
Related	also

ClinVar
Risk	rs121908674(G;G)
Alt	rs121908674(G;G)
Reference	Rs121908674(C;C)
Significance	Pathogenic
Disease	Exudative vitreoretinopathy 4
Variation	info
Gene	LRP5
CLNDBN	Exudative vitreoretinopathy 4, autosomal recessive
Reversed	0
HGVS	NC_000011.9:g.68177544C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006670.2,