Have questions? Visit https://www.reddit.com/r/SNPedia

rs7869550

From SNPedia

Orientationplus
Stabilizedplus
Make rs7869550(A;A)
Make rs7869550(A;G)
Make rs7869550(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position116372517
GenePAPPA
is asnp
is mentioned by
dbSNPrs7869550
ebirs7869550
HLIrs7869550
Exacrs7869550
Varsomers7869550
Maprs7869550
PheGenIrs7869550
hapmaprs7869550
1000 genomesrs7869550
hgdprs7869550
ensemblrs7869550
gopubmedrs7869550
geneviewrs7869550
scholarrs7869550
googlers7869550
pharmgkbrs7869550
gwascentralrs7869550
openSNPrs7869550
23andMers7869550
23andMe allrs7869550
SNP Nexus

SNPshotrs7869550
SNPdbers7869550
MSV3drs7869550
GWAS Ctlgrs7869550
GMAF0.09688
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18391950OA-icon.png]
Trait Height
Title Identification of ten loci associated with height highlights new biological pathways in human growth
Risk Allele G
P-val 9.9999999999999995E-7
Odds Ratio 0.33 [0.45-0.82] cm shorter


GET Evidence
rs7869550
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.117188
summary