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rs659822

From SNPedia

Orientationplus
Stabilizedplus
Make rs659822(C;C)
Make rs659822(C;T)
Make rs659822(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position62363592
GeneLAMA5
is asnp
is mentioned by
dbSNPrs659822
ebirs659822
HLIrs659822
Exacrs659822
Varsomers659822
Maprs659822
PheGenIrs659822
hapmaprs659822
1000 genomesrs659822
hgdprs659822
ensemblrs659822
gopubmedrs659822
geneviewrs659822
scholarrs659822
googlers659822
pharmgkbrs659822
gwascentralrs659822
openSNPrs659822
23andMers659822
23andMe allrs659822
SNP Nexus

SNPshotrs659822
SNPdbers659822
MSV3drs659822
GWAS Ctlgrs659822
GMAF0.2691
Max Magnitude
? (C;C) (C;T) (T;T) 28
news rs659822 was associated with weight (EA: P = 0.008; AA: P = 0.05) and lean mass (EA: P= 0.003; AA: P = 0.03), height (P = 0.01), total fat mass (P = 0.01), and HDL-cholesterol (P = 0.003).


[PMID 20951195OA-icon.png] Association of a common LAMA5 variant with anthropometric and metabolic traits in an Italian cohort of healthy elderly subjects


[PMID 18694491OA-icon.png] Genetic variation in a member of the laminin gene family affects variation in body composition in Drosophila and humans.