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rs7153027

From SNPedia

Orientationplus
Stabilizedplus
Make rs7153027(A;A)
Make rs7153027(A;C)
Make rs7153027(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position91960878
is asnp
is mentioned by
dbSNPrs7153027
ebirs7153027
HLIrs7153027
Exacrs7153027
Varsomers7153027
Maprs7153027
PheGenIrs7153027
hapmaprs7153027
1000 genomesrs7153027
hgdprs7153027
ensemblrs7153027
gopubmedrs7153027
geneviewrs7153027
scholarrs7153027
googlers7153027
pharmgkbrs7153027
gwascentralrs7153027
openSNPrs7153027
23andMers7153027
23andMe allrs7153027
SNP Nexus

SNPshotrs7153027
SNPdbers7153027
MSV3drs7153027
GWAS Ctlgrs7153027
GMAF0.3815
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele A
P-val 1E-10
Odds Ratio 5.70 [3.94-7.46] % SD taller


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


[PMID 19197348OA-icon.png] Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.


[PMID 20017971OA-icon.png] Assessing the impact of global versus local ancestry in association studies.


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


GET Evidence
rs7153027
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.4375
summary