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

rs139909

From SNPedia

Orientationplus
Stabilizedplus
Make rs139909(C;C)
Make rs139909(C;T)
Make rs139909(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position40301577
GeneTNRC6B
is asnp
is mentioned by
dbSNPrs139909
ebirs139909
HLIrs139909
Exacrs139909
Varsomers139909
Maprs139909
PheGenIrs139909
hapmaprs139909
1000 genomesrs139909
hgdprs139909
ensemblrs139909
gopubmedrs139909
geneviewrs139909
scholarrs139909
googlers139909
pharmgkbrs139909
gwascentralrs139909
openSNPrs139909
23andMers139909
23andMe allrs139909
SNP Nexus

SNPshotrs139909
SNPdbers139909
MSV3drs139909
GWAS Ctlgrs139909
GMAF0.3186
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19570815OA-icon.png]
Trait Height
Title A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation
Risk Allele T
P-val 2E-7
Odds Ratio 0.25 [0.03-0.47] cm increase


GET Evidence
rs139909
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.753968
summary