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rs7116722

From SNPedia

Orientationplus
Stabilizedplus
Make rs7116722(A;A)
Make rs7116722(A;C)
Make rs7116722(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position58739435
is asnp
is mentioned by
dbSNPrs7116722
ebirs7116722
HLIrs7116722
Exacrs7116722
Varsomers7116722
Maprs7116722
PheGenIrs7116722
hapmaprs7116722
1000 genomesrs7116722
hgdprs7116722
ensemblrs7116722
gopubmedrs7116722
geneviewrs7116722
scholarrs7116722
googlers7116722
pharmgkbrs7116722
gwascentralrs7116722
openSNPrs7116722
23andMers7116722
23andMe allrs7116722
SNP Nexus

SNPshotrs7116722
SNPdbers7116722
MSV3drs7116722
GWAS Ctlgrs7116722
GMAF0.03811
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 23108985OA-icon.png] Suggestion of GLYAT gene underlying variation of bone size and body lean mass as revealed by a bivariate genome-wide association study