Have questions? Visit https://www.reddit.com/r/SNPedia

rs6899976

From SNPedia

Orientationplus
Stabilizedplus
Make rs6899976(A;A)
Make rs6899976(A;G)
Make rs6899976(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position130037283
GeneL3MBTL3
is asnp
is mentioned by
dbSNPrs6899976
ebirs6899976
HLIrs6899976
Exacrs6899976
Varsomers6899976
Maprs6899976
PheGenIrs6899976
hapmaprs6899976
1000 genomesrs6899976
hgdprs6899976
ensemblrs6899976
gopubmedrs6899976
geneviewrs6899976
scholarrs6899976
googlers6899976
pharmgkbrs6899976
gwascentralrs6899976
openSNPrs6899976
23andMers6899976
23andMe allrs6899976
SNP Nexus

SNPshotrs6899976
SNPdbers6899976
MSV3drs6899976
GWAS Ctlgrs6899976
GMAF0.4224
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele G
P-val 0.0000060000000000000002
Odds Ratio 3.80 [2.23-5.37] % SD taller


GET Evidence
rs6899976
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.429688
summary