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rs10486607

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs10486607(C;T)
Make rs10486607(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position29144873
GeneCPVL, LOC644086
is asnp
is mentioned by
dbSNPrs10486607
ebirs10486607
HLIrs10486607
Exacrs10486607
Varsomers10486607
Maprs10486607
PheGenIrs10486607
hapmaprs10486607
1000 genomesrs10486607
hgdprs10486607
ensemblrs10486607
gopubmedrs10486607
geneviewrs10486607
scholarrs10486607
googlers10486607
pharmgkbrs10486607
gwascentralrs10486607
openSNPrs10486607
23andMers10486607
23andMe allrs10486607
SNP Nexus

SNPshotrs10486607
SNPdbers10486607
MSV3drs10486607
GWAS Ctlgrs10486607
GMAF0.1024
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903298OA-icon.png]
Trait Diabetes related insulin traits
Title Genome-wide association with diabetes-related traits in the Framingham Heart Study
Risk Allele
P-val 0.0000079999999999999996
Odds Ratio NR NR


GET Evidence
rs10486607
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.15625
summary