rs121918313

Orientation

minus

Stabilized

minus

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

Make rs121918313(C;T)

Make rs121918313(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

12164494

Gene

LRP6

is a	snp
is	mentioned by
dbSNP	rs121918313
dbSNP (classic)	rs121918313
ClinGen	rs121918313
ebi	rs121918313
HLI	rs121918313
Exac	rs121918313
Gnomad	rs121918313
Varsome	rs121918313
LitVar	rs121918313
Map	rs121918313
PheGenI	rs121918313
Biobank	rs121918313
1000 genomes	rs121918313
hgdp	rs121918313
ensembl	rs121918313
geneview	rs121918313
scholar	rs121918313
google	rs121918313
pharmgkb	rs121918313
gwascentral	rs121918313
openSNP	rs121918313
23andMe	rs121918313
SNPshot	rs121918313
SNPdbe	rs121918313
MSV3d	rs121918313
GWAS Ctlg	rs121918313

Max Magnitude

0

OMIM	603507
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121918313(T;T)
Alt	rs121918313(T;T)
Reference	Rs121918313(C;C)
Significance	Pathogenic
Disease	Coronary artery disease
Variation	info
Gene	LRP6
CLNDBN	Coronary artery disease, autosomal dominant 2
Reversed	1
HGVS	NC_000012.11:g.12317428G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006645.3,