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rs889014

From SNPedia

Orientationplus
Stabilizedplus
Make rs889014(C;C)
Make rs889014(C;T)
Make rs889014(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position173557111
is asnp
is mentioned by
dbSNPrs889014
ebirs889014
HLIrs889014
Exacrs889014
Varsomers889014
Maprs889014
PheGenIrs889014
hapmaprs889014
1000 genomesrs889014
hgdprs889014
ensemblrs889014
gopubmedrs889014
geneviewrs889014
scholarrs889014
googlers889014
pharmgkbrs889014
gwascentralrs889014
openSNPrs889014
23andMers889014
23andMe allrs889014
SNP Nexus

SNPshotrs889014
SNPdbers889014
MSV3drs889014
GWAS Ctlgrs889014
GMAF0.3623
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 9E-16
Odds Ratio .03 [NR] unit decrease