rs11669576

Orientation

plus

Stabilized

plus

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

Make rs11669576(A;A)

Make rs11669576(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

11111624

Gene	LDLR, MIR6886

is a	snp
is	mentioned by
dbSNP	rs11669576
dbSNP (classic)	rs11669576
ClinGen	rs11669576
ebi	rs11669576
HLI	rs11669576
Exac	rs11669576
Gnomad	rs11669576
Varsome	rs11669576
LitVar	rs11669576
Map	rs11669576
PheGenI	rs11669576
Biobank	rs11669576
1000 genomes	rs11669576
hgdp	rs11669576
ensembl	rs11669576
geneview	rs11669576
scholar	rs11669576
google	rs11669576
pharmgkb	rs11669576
gwascentral	rs11669576
openSNP	rs11669576
23andMe	rs11669576
SNPshot	rs11669576
SNPdbe	rs11669576
MSV3d	rs11669576
GWAS Ctlg	rs11669576

GMAF

0.07576

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 22050757] Functional non-synonymous polymorphisms prediction methods: current approaches and future developments

[PMID 17239995] Genetic study evaluating LDLR polymorphisms and Alzheimer's disease.

ClinVar
Risk	rs11669576(A;A)
Alt	rs11669576(A;A)
Reference	Rs11669576(G;G)
Significance	Other
Disease	not provided Familial hypercholesterolemia not specified
Variation	info
Gene	LDLR MIR6886
CLNDBN	not provided Familial hypercholesterolemia not specified
Reversed	0
HGVS	NC_000019.9:g.11222300G>A
CLNSRC	LDLR @ LOVD UniProtKB (protein)
CLNACC	RCV000162023.1, RCV000237576.4, RCV000241875.2,