rs121908665

Orientation

plus

Stabilized

plus

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

Make rs121908665(C;T)

Make rs121908665(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

68403606

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs121908665
dbSNP (classic)	rs121908665
ClinGen	rs121908665
ebi	rs121908665
HLI	rs121908665
Exac	rs121908665
Gnomad	rs121908665
Varsome	rs121908665
LitVar	rs121908665
Map	rs121908665
PheGenI	rs121908665
Biobank	rs121908665
1000 genomes	rs121908665
hgdp	rs121908665
ensembl	rs121908665
geneview	rs121908665
scholar	rs121908665
google	rs121908665
pharmgkb	rs121908665
gwascentral	rs121908665
openSNP	rs121908665
23andMe	rs121908665
SNPshot	rs121908665
SNPdbe	rs121908665
MSV3d	rs121908665
GWAS Ctlg	rs121908665

Max Magnitude

0

OMIM	603506
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121908665(T;T)
Alt	rs121908665(T;T)
Reference	Rs121908665(C;C)
Significance	Pathogenic
Disease	Osteoporosis with pseudoglioma
Variation	info
Gene	LRP5
CLNDBN	Osteoporosis with pseudoglioma
Reversed	0
HGVS	NC_000011.9:g.68171074C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006653.3,