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rs13043313

From SNPedia

Orientationplus
Stabilizedplus
Make rs13043313(C;C)
Make rs13043313(C;T)
Make rs13043313(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position62383213
is asnp
is mentioned by
dbSNPrs13043313
ebirs13043313
HLIrs13043313
Exacrs13043313
Varsomers13043313
Maprs13043313
PheGenIrs13043313
hapmaprs13043313
1000 genomesrs13043313
hgdprs13043313
ensemblrs13043313
gopubmedrs13043313
geneviewrs13043313
scholarrs13043313
googlers13043313
pharmgkbrs13043313
gwascentralrs13043313
openSNPrs13043313
23andMers13043313
23andMe allrs13043313
SNP Nexus

SNPshotrs13043313
SNPdbers13043313
MSV3drs13043313
GWAS Ctlgrs13043313
GMAF0.242
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20951195OA-icon.png] Association of a common LAMA5 variant with anthropometric and metabolic traits in an Italian cohort of healthy elderly subjects