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rs11958779

From SNPedia

Orientationplus
Stabilizedplus
Make rs11958779(A;A)
Make rs11958779(A;G)
Make rs11958779(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position55706071
GeneSLC38A9
is asnp
is mentioned by
dbSNPrs11958779
ebirs11958779
HLIrs11958779
Exacrs11958779
Varsomers11958779
Maprs11958779
PheGenIrs11958779
hapmaprs11958779
1000 genomesrs11958779
hgdprs11958779
ensemblrs11958779
gopubmedrs11958779
geneviewrs11958779
scholarrs11958779
googlers11958779
pharmgkbrs11958779
gwascentralrs11958779
openSNPrs11958779
23andMers11958779
23andMe allrs11958779
SNP Nexus

SNPshotrs11958779
SNPdbers11958779
MSV3drs11958779
GWAS Ctlgrs11958779
GMAF0.4284
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele A
P-val 2E-12
Odds Ratio 0.0300 [NR] meters decrease