rs2306029

Orientation

plus

Stabilized

plus

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

Make rs2306029(C;C)

Make rs2306029(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

46871557

Gene	LRP4, LRP4-AS1

is a	snp
is	mentioned by
dbSNP	rs2306029
dbSNP (classic)	rs2306029
ClinGen	rs2306029
ebi	rs2306029
HLI	rs2306029
Exac	rs2306029
Gnomad	rs2306029
Varsome	rs2306029
LitVar	rs2306029
Map	rs2306029
PheGenI	rs2306029
Biobank	rs2306029
1000 genomes	rs2306029
hgdp	rs2306029
ensembl	rs2306029
geneview	rs2306029
scholar	rs2306029
google	rs2306029
pharmgkb	rs2306029
gwascentral	rs2306029
openSNP	rs2306029
23andMe	rs2306029
SNPshot	rs2306029
SNPdbe	rs2306029
MSV3d	rs2306029
GWAS Ctlg	rs2306029

GMAF

0.3522

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 21121903] A variant of the LRP4 gene affects the risk of chronic lymphocytic leukaemia transformation to Richter syndrome

GWAS snp
PMID	[PMID 21502573]
Trait
Title	Genetic predictors of fibrin D-dimer levels in healthy adults.
Risk Allele	C
P-val	0.000008
Odds Ratio	0.0269 [NR] % decrease

[PMID 23321396] A common LRP4 haplotype is associated with bone mineral density and hip geometry in men-data from the Odense Androgen Study (OAS).

ClinVar
Risk	rs2306029(A;A) rs2306029(C;C)
Alt	rs2306029(A;A) rs2306029(C;C)
Reference	Rs2306029(T;T)
Significance	Non-pathogenic
Disease	Syndactyly Cenani Lenz type
Variation	info
Gene	LRP4-AS1 LRP4
CLNDBN	Syndactyly Cenani Lenz type
Reversed	0
HGVS	NC_000011.9:g.46893108T>C
CLNSRC
CLNACC	RCV000262910.1,