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rs798489

From SNPedia

Orientationminus
Stabilizedminus
Make rs798489(A;A)
Make rs798489(A;G)
Make rs798489(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position2762169
GeneGNA12
is asnp
is mentioned by
dbSNPrs798489
ebirs798489
HLIrs798489
Exacrs798489
Varsomers798489
Maprs798489
PheGenIrs798489
hapmaprs798489
1000 genomesrs798489
hgdprs798489
ensemblrs798489
gopubmedrs798489
geneviewrs798489
scholarrs798489
googlers798489
pharmgkbrs798489
gwascentralrs798489
openSNPrs798489
23andMers798489
23andMe allrs798489
SNP Nexus

SNPshotrs798489
SNPdbers798489
MSV3drs798489
GWAS Ctlgrs798489
GMAF0.1662
Max Magnitude
? (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-33
Odds Ratio .05 [NR] unit decrease