rs121908662

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(CTG;CTG)	0	common in clinvar

Make rs121908662(-;T)

Make rs121908662(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

68409973

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs121908662
dbSNP (classic)	rs121908662
ClinGen	rs121908662
ebi	rs121908662
HLI	rs121908662
Exac	rs121908662
Gnomad	rs121908662
Varsome	rs121908662
LitVar	rs121908662
Map	rs121908662
PheGenI	rs121908662
Biobank	rs121908662
1000 genomes	rs121908662
hgdp	rs121908662
ensembl	rs121908662
geneview	rs121908662
scholar	rs121908662
google	rs121908662
pharmgkb	rs121908662
gwascentral	rs121908662
openSNP	rs121908662
23andMe	rs121908662
SNPshot	rs121908662
SNPdbe	rs121908662
MSV3d	rs121908662
GWAS Ctlg	rs121908662

Max Magnitude

0

OMIM	603506
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121908662(T;T)
Alt	rs121908662(T;T)
Reference	Rs121908662(-;-)
Significance	Pathogenic
Disease	Osteoporosis with pseudoglioma
Variation	info
Gene	LRP5
CLNDBN	Osteoporosis with pseudoglioma
Reversed	0
HGVS	NC_000011.9:g.68177441dupT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006649.3,