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rs2154319

From SNPedia

Orientationplus
Stabilizedplus
Make rs2154319(C;C)
Make rs2154319(C;T)
Make rs2154319(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position41280098
is asnp
is mentioned by
dbSNPrs2154319
ebirs2154319
HLIrs2154319
Exacrs2154319
Varsomers2154319
Maprs2154319
PheGenIrs2154319
hapmaprs2154319
1000 genomesrs2154319
hgdprs2154319
ensemblrs2154319
gopubmedrs2154319
geneviewrs2154319
scholarrs2154319
googlers2154319
pharmgkbrs2154319
gwascentralrs2154319
openSNPrs2154319
23andMers2154319
23andMe allrs2154319
SNP Nexus

SNPshotrs2154319
SNPdbers2154319
MSV3drs2154319
GWAS Ctlgrs2154319
GMAF0.1111
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