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rs11177669

From SNPedia

Orientationplus
Stabilizedplus
Make rs11177669(A;A)
Make rs11177669(A;G)
Make rs11177669(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position69434901
is asnp
is mentioned by
dbSNPrs11177669
ebirs11177669
HLIrs11177669
Exacrs11177669
Varsomers11177669
Maprs11177669
PheGenIrs11177669
hapmaprs11177669
1000 genomesrs11177669
hgdprs11177669
ensemblrs11177669
gopubmedrs11177669
geneviewrs11177669
scholarrs11177669
googlers11177669
pharmgkbrs11177669
gwascentralrs11177669
openSNPrs11177669
23andMers11177669
23andMe allrs11177669
SNP Nexus

SNPshotrs11177669
SNPdbers11177669
MSV3drs11177669
GWAS Ctlgrs11177669
GMAF0.2938
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele A
P-val 0.0000030000000000000001
Odds Ratio 4.50 [2.54-6.46] % SD taller


GET Evidence
rs11177669
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.3125
summary