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rs212077

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs212077(C;G)
Make rs212077(G;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position16186919
GeneABCC6
is asnp
is mentioned by
dbSNPrs212077
ebirs212077
HLIrs212077
Exacrs212077
Varsomers212077
Maprs212077
PheGenIrs212077
hapmaprs212077
1000 genomesrs212077
hgdprs212077
ensemblrs212077
gopubmedrs212077
geneviewrs212077
scholarrs212077
googlers212077
pharmgkbrs212077
gwascentralrs212077
openSNPrs212077
23andMers212077
23andMe allrs212077
SNP Nexus

SNPshotrs212077
SNPdbers212077
MSV3drs212077
GWAS Ctlgrs212077
GMAF0.1171
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 20855565OA-icon.png] Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease
OMIM264800
Desc
Variant
Relatedalso


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 19750004OA-icon.png] A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia.