Have questions? Visit https://www.reddit.com/r/SNPedia

rs227724

From SNPedia

Orientationminus
Stabilizedminus
Make rs227724(A;A)
Make rs227724(A;T)
Make rs227724(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position56701456
is asnp
is mentioned by
dbSNPrs227724
dbSNP (classic)rs227724
ClinGenrs227724
ebirs227724
HLIrs227724
Exacrs227724
Gnomadrs227724
Varsomers227724
LitVarrs227724
Maprs227724
PheGenIrs227724
Biobankrs227724
1000 genomesrs227724
hgdprs227724
ensemblrs227724
geneviewrs227724
scholarrs227724
googlers227724
pharmgkbrs227724
gwascentralrs227724
openSNPrs227724
23andMers227724
SNPshotrs227724
SNPdbers227724
MSV3drs227724
GWAS Ctlgrs227724
GMAF0.2998
Max Magnitude0
? (A;A) (A;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 A
P-val 7E-15
Odds Ratio .03 [NR] unit decrease