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rs1052483

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1052483(A;A)
Make rs1052483(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position219069626
is asnp
is mentioned by
dbSNPrs1052483
ebirs1052483
HLIrs1052483
Exacrs1052483
Varsomers1052483
Maprs1052483
PheGenIrs1052483
hapmaprs1052483
1000 genomesrs1052483
hgdprs1052483
ensemblrs1052483
gopubmedrs1052483
geneviewrs1052483
scholarrs1052483
googlers1052483
pharmgkbrs1052483
gwascentralrs1052483
openSNPrs1052483
23andMers1052483
23andMe allrs1052483
SNP Nexus

SNPshotrs1052483
SNPdbers1052483
MSV3drs1052483
GWAS Ctlgrs1052483
GMAF0.1286
Max Magnitude0
? (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 C
P-val 9.9999999999999995E-7
Odds Ratio 6.90 [4.16-9.64] % 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
rs1052483
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.140625
summary