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rs473902

From SNPedia

Orientationminus
Stabilizedplus
Make rs473902(A;A)
Make rs473902(A;C)
Make rs473902(C;C)
ReferenceGRCh38 38.1/142
Chromosome9
Position95493953
GenePTCH1
is asnp
is mentioned by
dbSNPrs473902
ebirs473902
HLIrs473902
Exacrs473902
Varsomers473902
Maprs473902
PheGenIrs473902
hapmaprs473902
1000 genomesrs473902
hgdprs473902
ensemblrs473902
gopubmedrs473902
geneviewrs473902
scholarrs473902
googlers473902
pharmgkbrs473902
gwascentralrs473902
openSNPrs473902
23andMers473902
23andMe allrs473902
SNP Nexus

SNPshotrs473902
SNPdbers473902
MSV3drs473902
GWAS Ctlgrs473902
GMAF0.0326
Max Magnitude
? (A;A) (A;C) (C;C) 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-17
Odds Ratio .07 [NR] unit increase