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rs788867

From SNPedia

Orientationminus
Stabilizedplus
Make rs788867(A;A)
Make rs788867(A;C)
Make rs788867(C;C)
ReferenceGRCh38 38.1/142
Chromosome4
Position81228852
is asnp
is mentioned by
dbSNPrs788867
ebirs788867
HLIrs788867
Exacrs788867
Varsomers788867
Maprs788867
PheGenIrs788867
hapmaprs788867
1000 genomesrs788867
hgdprs788867
ensemblrs788867
gopubmedrs788867
geneviewrs788867
scholarrs788867
googlers788867
pharmgkbrs788867
gwascentralrs788867
openSNPrs788867
23andMers788867
23andMe allrs788867
SNP Nexus

SNPshotrs788867
SNPdbers788867
MSV3drs788867
GWAS Ctlgrs788867
GMAF0.3623
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 9E-28
Odds Ratio 0.04 [NR] unit decrease