Rs10515148

From SNPedia
Jump to: navigation, search

Orientationplus
Make rs10515148(C;C)
Make rs10515148(C;G)
Make rs10515148(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position72421101
is asnp
is mentioned by
dbSNPrs10515148
Exacrs10515148
PheGenIrs10515148
nextbiors10515148
hapmaprs10515148
1000 genomesrs10515148
hgdprs10515148
ensemblrs10515148
gopubmedrs10515148
geneviewrs10515148
scholarrs10515148
googlers10515148
pharmgkbrs10515148
gwascentralrs10515148
openSNPrs10515148
23andMers10515148
23andMe allrs10515148
SNP Nexus

SNPshotrs10515148
SNPdbers10515148
MSV3drs10515148
GMAF0.1864
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 17903296OA-icon.png]
Trait Hip geometry
Title Genome-wide association with bone mass and geometry in the Framingham Heart Study
Risk Allele
P-val 5.9999999999999997E-7
Odds Ratio NR NR


GET Evidence
rs10515148
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary