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rs6569648

From SNPedia

Orientationplus
Stabilizedplus
Make rs6569648(C;C)
Make rs6569648(C;T)
Make rs6569648(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position130027974
GeneL3MBTL3
is asnp
is mentioned by
dbSNPrs6569648
ebirs6569648
HLIrs6569648
Exacrs6569648
Varsomers6569648
Maprs6569648
PheGenIrs6569648
hapmaprs6569648
1000 genomesrs6569648
hgdprs6569648
ensemblrs6569648
gopubmedrs6569648
geneviewrs6569648
scholarrs6569648
googlers6569648
pharmgkbrs6569648
gwascentralrs6569648
openSNPrs6569648
23andMers6569648
23andMe allrs6569648
SNP Nexus

SNPshotrs6569648
SNPdbers6569648
MSV3drs6569648
GWAS Ctlgrs6569648
GMAF0.1212
Max Magnitude
? (C;C) (C;T) (T;T) 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 1E-21
Odds Ratio 0.04 [NR] unit decrease

[PMID 21757498OA-icon.png] Adult height variants affect birth length and growth rate in children.