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rs1590305

From SNPedia

Orientationminus
Stabilizedminus
Make rs1590305(A;A)
Make rs1590305(A;G)
Make rs1590305(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position37461052
is asnp
is mentioned by
dbSNPrs1590305
ebirs1590305
HLIrs1590305
Exacrs1590305
Varsomers1590305
Maprs1590305
PheGenIrs1590305
hapmaprs1590305
1000 genomesrs1590305
hgdprs1590305
ensemblrs1590305
gopubmedrs1590305
geneviewrs1590305
scholarrs1590305
googlers1590305
pharmgkbrs1590305
gwascentralrs1590305
openSNPrs1590305
23andMers1590305
23andMe allrs1590305
SNP Nexus

SNPshotrs1590305
SNPdbers1590305
MSV3drs1590305
GWAS Ctlgrs1590305
GMAF0.2415
Max Magnitude
? (A;A) (A;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 0.0000030000000000000001
Odds Ratio NR NR


GET Evidence
rs1590305
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.214286
summary