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rs150468

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs150468(A;C)
Make rs150468(C;C)
ReferenceGRCh38 38.1/142
Chromosome16
Position16158143
GeneABCC6
is asnp
is mentioned by
dbSNPrs150468
ebirs150468
HLIrs150468
Exacrs150468
Varsomers150468
Maprs150468
PheGenIrs150468
hapmaprs150468
1000 genomesrs150468
hgdprs150468
ensemblrs150468
gopubmedrs150468
geneviewrs150468
scholarrs150468
googlers150468
pharmgkbrs150468
gwascentralrs150468
openSNPrs150468
23andMers150468
23andMe allrs150468
SNP Nexus

SNPshotrs150468
SNPdbers150468
MSV3drs150468
GWAS Ctlgrs150468
GMAF0.1033
Max Magnitude0
? (A;A) (A;C) (C;C) 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 rs150468(C;C)
Alt rs150468(C;C)
Reference rs150468(A;A)
Significance Untested
Disease
Variation info
Gene ABCC6
CLNDBN
Reversed 1
HGVS NC_000016.9:g.16252000T>G
CLNSRC
CLNACC