rs397514664

Orientation

plus

Stabilized

plus

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

Make rs397514664(C;T)

Make rs397514664(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

68386445

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs397514664
dbSNP (classic)	rs397514664
ClinGen	rs397514664
ebi	rs397514664
HLI	rs397514664
Exac	rs397514664
Gnomad	rs397514664
Varsome	rs397514664
LitVar	rs397514664
Map	rs397514664
PheGenI	rs397514664
Biobank	rs397514664
1000 genomes	rs397514664
hgdp	rs397514664
ensembl	rs397514664
geneview	rs397514664
scholar	rs397514664
google	rs397514664
pharmgkb	rs397514664
gwascentral	rs397514664
openSNP	rs397514664
23andMe	rs397514664
SNPshot	rs397514664
SNPdbe	rs397514664
MSV3d	rs397514664
GWAS Ctlg	rs397514664

Max Magnitude

0

ClinVar
Risk	rs397514664(T;T)
Alt	rs397514664(T;T)
Reference	Rs397514664(C;C)
Significance	Pathogenic
Disease	Osteoporosis with pseudoglioma
Variation	info
Gene	LRP5
CLNDBN	Osteoporosis with pseudoglioma
Reversed	0
HGVS	NC_000011.9:g.68153913C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000033258.3,