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rs754388

From SNPedia

Orientationplus
Stabilizedplus
Make rs754388(C;C)
Make rs754388(C;G)
Make rs754388(G;G)
ReferenceGRCh38 38.1/142
Chromosome14
Position92649065
GeneRIN3
is asnp
is mentioned by
dbSNPrs754388
ebirs754388
HLIrs754388
Exacrs754388
Varsomers754388
Maprs754388
PheGenIrs754388
hapmaprs754388
1000 genomesrs754388
hgdprs754388
ensemblrs754388
gopubmedrs754388
geneviewrs754388
scholarrs754388
googlers754388
pharmgkbrs754388
gwascentralrs754388
openSNPrs754388
23andMers754388
23andMe allrs754388
SNP Nexus

SNPshotrs754388
SNPdbers754388
MSV3drs754388
GWAS Ctlgrs754388
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 24621683OA-icon.png]
Trait Chronic obstructive pulmonary disease (moderate to severe)
Title Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.
Risk Allele C
P-val 5E-9
Odds Ratio NR NR
GWAS snp
PMID [PMID 24945404OA-icon.png]
Trait Bone mineral density (paediatric, lower limb)
Title Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.
Risk Allele C
P-val 1E-10
Odds Ratio .13 [0.091-0.169] unit increase