rs397514665

Orientation

plus

Stabilized

plus

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

Make rs397514665(C;T)

Make rs397514665(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

68363791

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs397514665
dbSNP (classic)	rs397514665
ClinGen	rs397514665
ebi	rs397514665
HLI	rs397514665
Exac	rs397514665
Gnomad	rs397514665
Varsome	rs397514665
LitVar	rs397514665
Map	rs397514665
PheGenI	rs397514665
Biobank	rs397514665
1000 genomes	rs397514665
hgdp	rs397514665
ensembl	rs397514665
geneview	rs397514665
scholar	rs397514665
google	rs397514665
pharmgkb	rs397514665
gwascentral	rs397514665
openSNP	rs397514665
23andMe	rs397514665
SNPshot	rs397514665
SNPdbe	rs397514665
MSV3d	rs397514665
GWAS Ctlg	rs397514665

Max Magnitude

0

ClinVar
Risk	rs397514665(T;T)
Alt	rs397514665(T;T)
Reference	Rs397514665(C;C)
Significance	Pathogenic
Disease	Osteoporosis with pseudoglioma
Variation	info
Gene	LRP5
CLNDBN	Osteoporosis with pseudoglioma
Reversed	0
HGVS	NC_000011.9:g.68131259C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000033259.4,