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rs6938239

From SNPedia

Orientationplus
Stabilizedplus
Make rs6938239(A;A)
Make rs6938239(A;G)
Make rs6938239(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position34715858
is asnp
is mentioned by
dbSNPrs6938239
ebirs6938239
HLIrs6938239
Exacrs6938239
Varsomers6938239
Maprs6938239
PheGenIrs6938239
hapmaprs6938239
1000 genomesrs6938239
hgdprs6938239
ensemblrs6938239
gopubmedrs6938239
geneviewrs6938239
scholarrs6938239
googlers6938239
pharmgkbrs6938239
gwascentralrs6938239
openSNPrs6938239
23andMers6938239
23andMe allrs6938239
SNP Nexus

SNPshotrs6938239
SNPdbers6938239
MSV3drs6938239
GWAS Ctlgrs6938239
GMAF0.1116
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
P-val 6E-12
Odds Ratio NR NR