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rs10496265

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs10496265(A;G)
Make rs10496265(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position81441684
is asnp
is mentioned by
dbSNPrs10496265
ebirs10496265
HLIrs10496265
Exacrs10496265
Varsomers10496265
Maprs10496265
PheGenIrs10496265
hapmaprs10496265
1000 genomesrs10496265
hgdprs10496265
ensemblrs10496265
gopubmedrs10496265
geneviewrs10496265
scholarrs10496265
googlers10496265
pharmgkbrs10496265
gwascentralrs10496265
openSNPrs10496265
23andMers10496265
23andMe allrs10496265
SNP Nexus

SNPshotrs10496265
SNPdbers10496265
MSV3drs10496265
GWAS Ctlgrs10496265
GMAF0.07943
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs10496265
PubMedID [PMID 17903295OA-icon.png]
Condition Aging traits
Gene Intergenic
Risk Allele
pValue 1.00E-008
OR NA
95% CI



GET Evidence
rs10496265
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.078125
summary