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rs1490388

From SNPedia

Orientationplus
Stabilizedplus
Make rs1490388(C;C)
Make rs1490388(C;T)
Make rs1490388(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position126514509
is asnp
is mentioned by
dbSNPrs1490388
ebirs1490388
HLIrs1490388
Exacrs1490388
Varsomers1490388
Maprs1490388
PheGenIrs1490388
hapmaprs1490388
1000 genomesrs1490388
hgdprs1490388
ensemblrs1490388
gopubmedrs1490388
geneviewrs1490388
scholarrs1490388
googlers1490388
pharmgkbrs1490388
gwascentralrs1490388
openSNPrs1490388
23andMers1490388
23andMe allrs1490388
SNP Nexus

SNPshotrs1490388
SNPdbers1490388
MSV3drs1490388
GWAS Ctlgrs1490388
GMAF0.4389
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 5.9999999999999997E-7
Odds Ratio 4.80 [2.84-6.76] % SD taller


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


GET Evidence
rs1490388
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.507936
summary