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rs2274432

From SNPedia

Orientationminus
Stabilizedminus
Make rs2274432(C;C)
Make rs2274432(C;T)
Make rs2274432(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position184051811
GeneTSEN15
is asnp
is mentioned by
dbSNPrs2274432
ebirs2274432
HLIrs2274432
Exacrs2274432
Varsomers2274432
Maprs2274432
PheGenIrs2274432
hapmaprs2274432
1000 genomesrs2274432
hgdprs2274432
ensemblrs2274432
gopubmedrs2274432
geneviewrs2274432
scholarrs2274432
googlers2274432
pharmgkbrs2274432
gwascentralrs2274432
openSNPrs2274432
23andMers2274432
23andMe allrs2274432
SNP Nexus

SNPshotrs2274432
SNPdbers2274432
MSV3drs2274432
GWAS Ctlgrs2274432
GMAF0.3223
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele T
P-val 8.0000000000000005E-9
Odds Ratio 5.30 [3.54-7.06] % SD taller


[PMID 19474294OA-icon.png] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.


[PMID 20546612OA-icon.png] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.


GET Evidence
TSEN15-G19D
aa_change Gly19Asp
aa_change_short G19D
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.241233
summary