rs397515473

Orientation

minus

Stabilized

minus

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

Make rs397515473(A;G)

Make rs397515473(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

12181118

Gene

LRP6

is a	snp
is	mentioned by
dbSNP	rs397515473
dbSNP (classic)	rs397515473
ClinGen	rs397515473
ebi	rs397515473
HLI	rs397515473
Exac	rs397515473
Gnomad	rs397515473
Varsome	rs397515473
LitVar	rs397515473
Map	rs397515473
PheGenI	rs397515473
Biobank	rs397515473
1000 genomes	rs397515473
hgdp	rs397515473
ensembl	rs397515473
geneview	rs397515473
scholar	rs397515473
google	rs397515473
pharmgkb	rs397515473
gwascentral	rs397515473
openSNP	rs397515473
23andMe	rs397515473
SNPshot	rs397515473
SNPdbe	rs397515473
MSV3d	rs397515473
GWAS Ctlg	rs397515473

Max Magnitude

0

ClinVar
Risk	rs397515473(G;G)
Alt	rs397515473(G;G)
Reference	Rs397515473(A;A)
Significance	Pathogenic
Disease	Coronary artery disease
Variation	info
Gene	LRP6
CLNDBN	Coronary artery disease, autosomal dominant 2
Reversed	1
HGVS	NC_000012.11:g.12334052T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000056292.2,