rs387906884

Orientation

minus

Stabilized

minus

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

Make rs387906884(C;T)

Make rs387906884(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

46876494

Gene

LRP4

is a	snp
is	mentioned by
dbSNP	rs387906884
dbSNP (classic)	rs387906884
ClinGen	rs387906884
ebi	rs387906884
HLI	rs387906884
Exac	rs387906884
Gnomad	rs387906884
Varsome	rs387906884
LitVar	rs387906884
Map	rs387906884
PheGenI	rs387906884
Biobank	rs387906884
1000 genomes	rs387906884
hgdp	rs387906884
ensembl	rs387906884
geneview	rs387906884
scholar	rs387906884
google	rs387906884
pharmgkb	rs387906884
gwascentral	rs387906884
openSNP	rs387906884
23andMe	rs387906884
SNPshot	rs387906884
SNPdbe	rs387906884
MSV3d	rs387906884
GWAS Ctlg	rs387906884

Max Magnitude

0

ClinVar
Risk	rs387906884(T;T)
Alt	rs387906884(T;T)
Reference	Rs387906884(C;C)
Significance	Pathogenic
Disease	Sclerosteosis 2
Variation	info
Gene	LRP4
CLNDBN	Sclerosteosis 2
Reversed	1
HGVS	NC_000011.9:g.46898045G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023364.3,