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rs10507130

From SNPedia

Orientationplus
Stabilizedplus
Make rs10507130(A;A)
Make rs10507130(A;G)
Make rs10507130(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position101360176
GeneUTP20
is asnp
is mentioned by
dbSNPrs10507130
ebirs10507130
HLIrs10507130
Exacrs10507130
Varsomers10507130
Maprs10507130
PheGenIrs10507130
hapmaprs10507130
1000 genomesrs10507130
hgdprs10507130
ensemblrs10507130
gopubmedrs10507130
geneviewrs10507130
scholarrs10507130
googlers10507130
pharmgkbrs10507130
gwascentralrs10507130
openSNPrs10507130
23andMers10507130
23andMe allrs10507130
SNP Nexus

SNPshotrs10507130
SNPdbers10507130
MSV3drs10507130
GWAS Ctlgrs10507130
GMAF0.2337
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903303OA-icon.png]
Trait Coronary artery calcification
Title Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study
Risk Allele
P-val 0.0000069999999999999999
Odds Ratio NR NR


GET Evidence
rs10507130
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.117188
summary