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

rs1013209

From SNPedia

Orientationplus
Stabilizedplus
Make rs1013209(C;C)
Make rs1013209(C;T)
Make rs1013209(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position24258791
is asnp
is mentioned by
dbSNPrs1013209
ebirs1013209
HLIrs1013209
Exacrs1013209
Varsomers1013209
Maprs1013209
PheGenIrs1013209
hapmaprs1013209
1000 genomesrs1013209
hgdprs1013209
ensemblrs1013209
gopubmedrs1013209
geneviewrs1013209
scholarrs1013209
googlers1013209
pharmgkbrs1013209
gwascentralrs1013209
openSNPrs1013209
23andMers1013209
23andMe allrs1013209
SNP Nexus

SNPshotrs1013209
SNPdbers1013209
MSV3drs1013209
GWAS Ctlgrs1013209
GMAF0.3049
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 2E-9
Odds Ratio 0.0300 [NR] meters decrease