rs121908664

Orientation

plus

Stabilized

plus

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

Make rs121908664(A;A)

Make rs121908664(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

68389949

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs121908664
dbSNP (classic)	rs121908664
ClinGen	rs121908664
ebi	rs121908664
HLI	rs121908664
Exac	rs121908664
Gnomad	rs121908664
Varsome	rs121908664
LitVar	rs121908664
Map	rs121908664
PheGenI	rs121908664
Biobank	rs121908664
1000 genomes	rs121908664
hgdp	rs121908664
ensembl	rs121908664
geneview	rs121908664
scholar	rs121908664
google	rs121908664
pharmgkb	rs121908664
gwascentral	rs121908664
openSNP	rs121908664
23andMe	rs121908664
SNPshot	rs121908664
SNPdbe	rs121908664
MSV3d	rs121908664
GWAS Ctlg	rs121908664

Max Magnitude

0

OMIM	603506
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121908664(A;A)
Alt	rs121908664(A;A)
Reference	Rs121908664(G;G)
Significance	Pathogenic
Disease	Osteoporosis with pseudoglioma not provided
Variation	info
Gene	LRP5
CLNDBN	Osteoporosis with pseudoglioma not provided
Reversed	0
HGVS	NC_000011.9:g.68157417G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006652.3, RCV000414333.1,