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rs12199222

From SNPedia

Orientationplus
Stabilizedplus
Make rs12199222(G;G)
Make rs12199222(G;T)
Make rs12199222(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position17699091
GeneNUP153
is asnp
is mentioned by
dbSNPrs12199222
ebirs12199222
HLIrs12199222
Exacrs12199222
Varsomers12199222
Maprs12199222
PheGenIrs12199222
hapmaprs12199222
1000 genomesrs12199222
hgdprs12199222
ensemblrs12199222
gopubmedrs12199222
geneviewrs12199222
scholarrs12199222
googlers12199222
pharmgkbrs12199222
gwascentralrs12199222
openSNPrs12199222
23andMers12199222
23andMe allrs12199222
SNP Nexus

SNPshotrs12199222
SNPdbers12199222
MSV3drs12199222
GWAS Ctlgrs12199222
GMAF0.2704
Max Magnitude
? (G;G) (G;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 6.9999999999999997E-7
Odds Ratio 4.40 [2.64-6.16] % SD taller

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


GET Evidence
rs12199222
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.210938
summary