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rs10507577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs10507577(C;C)
Make rs10507577(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position53393956
is asnp
is mentioned by
dbSNPrs10507577
ebirs10507577
HLIrs10507577
Exacrs10507577
Varsomers10507577
Maprs10507577
PheGenIrs10507577
hapmaprs10507577
1000 genomesrs10507577
hgdprs10507577
ensemblrs10507577
gopubmedrs10507577
geneviewrs10507577
scholarrs10507577
googlers10507577
pharmgkbrs10507577
gwascentralrs10507577
openSNPrs10507577
23andMers10507577
23andMe allrs10507577
SNP Nexus

SNPshotrs10507577
SNPdbers10507577
MSV3drs10507577
GWAS Ctlgrs10507577
GMAF0.09596
Max Magnitude0
? (C;C) (C;T) (T;T) 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 0.0000030000000000000001
Odds Ratio NR NR


GET Evidence
rs10507577
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.129032
summary