rs212077

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs212077(C;G)

Make rs212077(G;G)

Reference

GRCh38 38.1/142

Chromosome

16

Position

16186919

Gene

ABCC6

is a	snp
is	mentioned by
dbSNP	rs212077
dbSNP (classic)	rs212077
ClinGen	rs212077
ebi	rs212077
HLI	rs212077
Exac	rs212077
Gnomad	rs212077
Varsome	rs212077
LitVar	rs212077
Map	rs212077
PheGenI	rs212077
Biobank	rs212077
1000 genomes	rs212077
hgdp	rs212077
ensembl	rs212077
geneview	rs212077
scholar	rs212077
google	rs212077
pharmgkb	rs212077
gwascentral	rs212077
openSNP	rs212077
23andMe	rs212077
SNPshot	rs212077
SNPdbe	rs212077
MSV3d	rs212077
GWAS Ctlg	rs212077

GMAF

0.1171

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

[PMID 20855565] Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease

OMIM	264800
Desc
Variant
Related	also

ClinVar
Risk	rs212077(G;G)
Alt	rs212077(G;G)
Reference	Rs212077(C;C)
Significance	Untested
Disease
Variation	info
Gene	ABCC6
CLNDBN
Reversed	1
HGVS	NC_000016.9:g.16280776G>C
CLNSRC
CLNACC

[PMID 19750004] A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia.