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rs2145272

From SNPedia

Orientationplus
Stabilizedplus
Make rs2145272(A;A)
Make rs2145272(A;G)
Make rs2145272(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position6645571
is asnp
is mentioned by
dbSNPrs2145272
ebirs2145272
HLIrs2145272
Exacrs2145272
Varsomers2145272
Maprs2145272
PheGenIrs2145272
hapmaprs2145272
1000 genomesrs2145272
hgdprs2145272
ensemblrs2145272
gopubmedrs2145272
geneviewrs2145272
scholarrs2145272
googlers2145272
pharmgkbrs2145272
gwascentralrs2145272
openSNPrs2145272
23andMers2145272
23andMe allrs2145272
SNP Nexus

SNPshotrs2145272
SNPdbers2145272
MSV3drs2145272
GWAS Ctlgrs2145272
GMAF0.292
Max Magnitude
? (A;A) (A;G) (G;G) 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 A
P-val 2E-24
Odds Ratio .04 [NR] unit decrease