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rs10485165

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs10485165(A;A)
Make rs10485165(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position88403098
is asnp
is mentioned by
dbSNPrs10485165
ebirs10485165
HLIrs10485165
Exacrs10485165
Varsomers10485165
Maprs10485165
PheGenIrs10485165
hapmaprs10485165
1000 genomesrs10485165
hgdprs10485165
ensemblrs10485165
gopubmedrs10485165
geneviewrs10485165
scholarrs10485165
googlers10485165
pharmgkbrs10485165
gwascentralrs10485165
openSNPrs10485165
23andMers10485165
23andMe allrs10485165
SNP Nexus

SNPshotrs10485165
SNPdbers10485165
MSV3drs10485165
GWAS Ctlgrs10485165
GMAF0.174
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903293OA-icon.png]
Trait Select biomarker traits
Title Genome-wide association with select biomarker traits in the Framingham Heart Study
Risk Allele
P-val 9.9999999999999995E-7
Odds Ratio NR NR

[PMID 17903293OA-icon.png] select biomarker trait being 25(OH) vitamin D plasma levels


GET Evidence
rs10485165
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary