rs121908661

Orientation

plus

Stabilized

plus

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

Make rs121908661(C;T)

Make rs121908661(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

68386582

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs121908661
dbSNP (classic)	rs121908661
ClinGen	rs121908661
ebi	rs121908661
HLI	rs121908661
Exac	rs121908661
Gnomad	rs121908661
Varsome	rs121908661
LitVar	rs121908661
Map	rs121908661
PheGenI	rs121908661
Biobank	rs121908661
1000 genomes	rs121908661
hgdp	rs121908661
ensembl	rs121908661
geneview	rs121908661
scholar	rs121908661
google	rs121908661
pharmgkb	rs121908661
gwascentral	rs121908661
openSNP	rs121908661
23andMe	rs121908661
SNPshot	rs121908661
SNPdbe	rs121908661
MSV3d	rs121908661
GWAS Ctlg	rs121908661

Max Magnitude

0

OMIM	603506
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121908661(T;T)
Alt	rs121908661(T;T)
Reference	Rs121908661(C;C)
Significance	Pathogenic
Disease	Osteoporosis with pseudoglioma
Variation	info
Gene	LRP5
CLNDBN	Osteoporosis with pseudoglioma
Reversed	0
HGVS	NC_000011.9:g.68154050C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006647.3,