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rs1173727

From SNPedia

Orientationminus
Stabilizedminus
Make rs1173727(A;A)
Make rs1173727(A;G)
Make rs1173727(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position32830415
is asnp
is mentioned by
dbSNPrs1173727
dbSNP (classic)rs1173727
ClinGenrs1173727
ebirs1173727
HLIrs1173727
Exacrs1173727
Gnomadrs1173727
Varsomers1173727
LitVarrs1173727
Maprs1173727
PheGenIrs1173727
Biobankrs1173727
1000 genomesrs1173727
hgdprs1173727
ensemblrs1173727
geneviewrs1173727
scholarrs1173727
googlers1173727
pharmgkbrs1173727
gwascentralrs1173727
openSNPrs1173727
23andMers1173727
SNPshotrs1173727
SNPdbers1173727
MSV3drs1173727
GWAS Ctlgrs1173727
GMAF0.3462
Max Magnitude0
? (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 T
P-val 2E-21
Odds Ratio .03 [NR] unit increase