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rs10105606

From SNPedia

Orientationplus
Stabilizedplus
Make rs10105606(A;A)
Make rs10105606(A;C)
Make rs10105606(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position19970337
is asnp
is mentioned by
dbSNPrs10105606
ebirs10105606
HLIrs10105606
Exacrs10105606
Varsomers10105606
Maprs10105606
PheGenIrs10105606
hapmaprs10105606
1000 genomesrs10105606
hgdprs10105606
ensemblrs10105606
gopubmedrs10105606
geneviewrs10105606
scholarrs10105606
googlers10105606
pharmgkbrs10105606
gwascentralrs10105606
openSNPrs10105606
23andMers10105606
23andMe allrs10105606
SNP Nexus

SNPshotrs10105606
SNPdbers10105606
MSV3drs10105606
GWAS Ctlgrs10105606
GMAF0.3788
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20864672OA-icon.png]
Trait
Title Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
Risk Allele C
P-val 4E-26
Odds Ratio 0.07 [0.06-0.08] increase


[PMID 19041386OA-icon.png] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.


[PMID 19148283OA-icon.png] Genetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart Study.


[PMID 23832694] Common genetic variants associated with lipid profiles in a Chinese pediatric population.