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rs2072153

From SNPedia

Orientationminus
Stabilizedminus
Make rs2072153(C;C)
Make rs2072153(C;G)
Make rs2072153(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position49312652
GeneZNF652
is asnp
is mentioned by
dbSNPrs2072153
ebirs2072153
HLIrs2072153
Exacrs2072153
Varsomers2072153
Maprs2072153
PheGenIrs2072153
hapmaprs2072153
1000 genomesrs2072153
hgdprs2072153
ensemblrs2072153
gopubmedrs2072153
geneviewrs2072153
scholarrs2072153
googlers2072153
pharmgkbrs2072153
gwascentralrs2072153
openSNPrs2072153
23andMers2072153
23andMe allrs2072153
SNP Nexus

SNPshotrs2072153
SNPdbers2072153
MSV3drs2072153
GWAS Ctlgrs2072153
GMAF0.3209
Max Magnitude
? (C;C) (C;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 C
P-val 4E-8
Odds Ratio .02 [NR] unit increase