rs121908663

Orientation

plus

Stabilized

plus

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

Make rs121908663(C;T)

Make rs121908663(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

68413742

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs121908663
dbSNP (classic)	rs121908663
ClinGen	rs121908663
ebi	rs121908663
HLI	rs121908663
Exac	rs121908663
Gnomad	rs121908663
Varsome	rs121908663
LitVar	rs121908663
Map	rs121908663
PheGenI	rs121908663
Biobank	rs121908663
1000 genomes	rs121908663
hgdp	rs121908663
ensembl	rs121908663
geneview	rs121908663
scholar	rs121908663
google	rs121908663
pharmgkb	rs121908663
gwascentral	rs121908663
openSNP	rs121908663
23andMe	rs121908663
SNPshot	rs121908663
SNPdbe	rs121908663
MSV3d	rs121908663
GWAS Ctlg	rs121908663

Max Magnitude

0

OMIM	603506
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121908663(T;T)
Alt	rs121908663(T;T)
Reference	Rs121908663(C;C)
Significance	Pathogenic
Disease	Osteoporosis with pseudoglioma
Variation	info
Gene	LRP5
CLNDBN	Osteoporosis with pseudoglioma
Reversed	0
HGVS	NC_000011.9:g.68181210C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006650.3,