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rs7567288

From SNPedia

Orientationplus
Stabilizedplus
Make rs7567288(C;C)
Make rs7567288(C;T)
Make rs7567288(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position133677253
is asnp
is mentioned by
dbSNPrs7567288
ebirs7567288
HLIrs7567288
Exacrs7567288
Varsomers7567288
Maprs7567288
PheGenIrs7567288
hapmaprs7567288
1000 genomesrs7567288
hgdprs7567288
ensemblrs7567288
gopubmedrs7567288
geneviewrs7567288
scholarrs7567288
googlers7567288
pharmgkbrs7567288
gwascentralrs7567288
openSNPrs7567288
23andMers7567288
23andMe allrs7567288
SNP Nexus

SNPshotrs7567288
SNPdbers7567288
MSV3drs7567288
GWAS Ctlgrs7567288
GMAF0.202
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 2E-12
Odds Ratio .03 [NR] unit decrease