rs121908672

Orientation

plus

Stabilized

plus

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

Make rs121908672(C;T)

Make rs121908672(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

68357802

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs121908672
dbSNP (classic)	rs121908672
ClinGen	rs121908672
ebi	rs121908672
HLI	rs121908672
Exac	rs121908672
Gnomad	rs121908672
Varsome	rs121908672
LitVar	rs121908672
Map	rs121908672
PheGenI	rs121908672
Biobank	rs121908672
1000 genomes	rs121908672
hgdp	rs121908672
ensembl	rs121908672
geneview	rs121908672
scholar	rs121908672
google	rs121908672
pharmgkb	rs121908672
gwascentral	rs121908672
openSNP	rs121908672
23andMe	rs121908672
SNPshot	rs121908672
SNPdbe	rs121908672
MSV3d	rs121908672
GWAS Ctlg	rs121908672

Max Magnitude

0

OMIM	603506
Desc
Variant	0017
Related	also

ClinVar
Risk	rs121908672(T;T)
Alt	rs121908672(T;T)
Reference	Rs121908672(C;C)
Significance	Pathogenic
Disease	Worth disease
Variation	info
Gene	LRP5
CLNDBN	Worth disease
Reversed	0
HGVS	NC_000011.9:g.68125270C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006664.2,