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rs991258

From SNPedia

Orientationminus
Stabilizedminus
Make rs991258(C;C)
Make rs991258(C;G)
Make rs991258(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position102055199
is asnp
is mentioned by
dbSNPrs991258
ebirs991258
HLIrs991258
Exacrs991258
Varsomers991258
Maprs991258
PheGenIrs991258
hapmaprs991258
1000 genomesrs991258
hgdprs991258
ensemblrs991258
gopubmedrs991258
geneviewrs991258
scholarrs991258
googlers991258
pharmgkbrs991258
gwascentralrs991258
openSNPrs991258
23andMers991258
23andMe allrs991258
SNP Nexus

SNPshotrs991258
SNPdbers991258
MSV3drs991258
GWAS Ctlgrs991258
GMAF0.3747
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 4.9999999999999998E-7
Odds Ratio NR NR


GET Evidence
rs991258
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.28125
summary