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rs17038182

From SNPedia

Orientationplus
Stabilizedplus
Make rs17038182(C;C)
Make rs17038182(C;G)
Make rs17038182(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position118325782
is asnp
is mentioned by
dbSNPrs17038182
ebirs17038182
HLIrs17038182
Exacrs17038182
Varsomers17038182
Maprs17038182
PheGenIrs17038182
hapmaprs17038182
1000 genomesrs17038182
hgdprs17038182
ensemblrs17038182
gopubmedrs17038182
geneviewrs17038182
scholarrs17038182
googlers17038182
pharmgkbrs17038182
gwascentralrs17038182
openSNPrs17038182
23andMers17038182
23andMe allrs17038182
SNP Nexus

SNPshotrs17038182
SNPdbers17038182
MSV3drs17038182
GWAS Ctlgrs17038182
GMAF0.2833
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19396169]
Trait Height
Title A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
Risk Allele C
P-val 5E-7
Odds Ratio 0.30 [0.18-0.42] cm decrease


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


GET Evidence
rs17038182
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.242188
summary