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rs10490626

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
Make rs10490626(C;T)
Make rs10490626(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position118078265
is asnp
is mentioned by
dbSNPrs10490626
ebirs10490626
HLIrs10490626
Exacrs10490626
Varsomers10490626
Maprs10490626
PheGenIrs10490626
hapmaprs10490626
1000 genomesrs10490626
hgdprs10490626
ensemblrs10490626
gopubmedrs10490626
geneviewrs10490626
scholarrs10490626
googlers10490626
pharmgkbrs10490626
gwascentralrs10490626
openSNPrs10490626
23andMers10490626
23andMe allrs10490626
SNP Nexus

SNPshotrs10490626
SNPdbers10490626
MSV3drs10490626
GWAS Ctlgrs10490626
GMAF0.03444
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 20858904] Fine Mapping of the INSIG2 Gene Identifies a Variant Associated with Low-Density Lipoprotein Cholesterol and Total ApoB Levels


[PMID 19360016OA-icon.png] INSIG2 SNPs associated with obesity and glucose homeostasis traits in Hispanics: the IRAS Family Study.

GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait Cholesterol, total
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele A
P-val 6E-9
Odds Ratio .04 [NR] unit increase