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rs1528753

From SNPedia

Orientationplus
Stabilizedplus
Make rs1528753(A;A)
Make rs1528753(A;C)
Make rs1528753(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position91151171
is asnp
is mentioned by
dbSNPrs1528753
ebirs1528753
HLIrs1528753
Exacrs1528753
Varsomers1528753
Maprs1528753
PheGenIrs1528753
hapmaprs1528753
1000 genomesrs1528753
hgdprs1528753
ensemblrs1528753
gopubmedrs1528753
geneviewrs1528753
scholarrs1528753
googlers1528753
pharmgkbrs1528753
gwascentralrs1528753
openSNPrs1528753
23andMers1528753
23andMe allrs1528753
SNP Nexus

SNPshotrs1528753
SNPdbers1528753
MSV3drs1528753
GWAS Ctlgrs1528753
GMAF0.3223
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS
SNP rs1528753
PubMedID [PMID 17903295OA-icon.png]
Condition Aging traits
Gene Intergenic
Risk Allele
pValue 8.00E-008
OR NA
95% CI



GET Evidence
rs1528753
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.701613
summary