rs121908671

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common genotype
(G;G)	0	common in clinvar

Make rs121908671(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

68357801

Gene

LRP5

is a	snp
is	mentioned by
dbSNP	rs121908671
dbSNP (classic)	rs121908671
ClinGen	rs121908671
ebi	rs121908671
HLI	rs121908671
Exac	rs121908671
Gnomad	rs121908671
Varsome	rs121908671
LitVar	rs121908671
Map	rs121908671
PheGenI	rs121908671
Biobank	rs121908671
1000 genomes	rs121908671
hgdp	rs121908671
ensembl	rs121908671
geneview	rs121908671
scholar	rs121908671
google	rs121908671
pharmgkb	rs121908671
gwascentral	rs121908671
openSNP	rs121908671
23andMe	rs121908671
SNPshot	rs121908671
SNPdbe	rs121908671
MSV3d	rs121908671
GWAS Ctlg	rs121908671

Max Magnitude

0

OMIM	603506
Desc
Variant	0016
Related	also

ClinVar
Risk	Rs121908671(A;A)
Alt	Rs121908671(A;A)
Reference	Rs121908671(G;G)
Significance	Pathogenic
Disease	Worth disease
Variation	info
Gene	LRP5
CLNDBN	Worth disease
Reversed	0
HGVS	NC_000011.9:g.68125269G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006663.2,