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rs9650315

From SNPedia

Orientationplus
Stabilizedplus
Make rs9650315(G;G)
Make rs9650315(G;T)
Make rs9650315(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position56243039
is asnp
is mentioned by
dbSNPrs9650315
ebirs9650315
HLIrs9650315
Exacrs9650315
Varsomers9650315
Maprs9650315
PheGenIrs9650315
hapmaprs9650315
1000 genomesrs9650315
hgdprs9650315
ensemblrs9650315
gopubmedrs9650315
geneviewrs9650315
scholarrs9650315
googlers9650315
pharmgkbrs9650315
gwascentralrs9650315
openSNPrs9650315
23andMers9650315
23andMe allrs9650315
SNP Nexus

SNPshotrs9650315
SNPdbers9650315
MSV3drs9650315
GWAS Ctlgrs9650315
GMAF0.1956
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 18391950OA-icon.png]
Trait Height
Title Identification of ten loci associated with height highlights new biological pathways in human growth
Risk Allele T
P-val 3.9999999999999998E-7
Odds Ratio 0.43 [0.59-1.07] cm shorter


[PMID 19030899OA-icon.png] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.


[PMID 20027299OA-icon.png] Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.


GET Evidence
rs9650315
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.226562
summary