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rs805136

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs805136(A;A)
Make rs805136(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position28045236
is asnp
is mentioned by
dbSNPrs805136
dbSNP (classic)rs805136
ClinGenrs805136
ebirs805136
HLIrs805136
Exacrs805136
Gnomadrs805136
Varsomers805136
LitVarrs805136
Maprs805136
PheGenIrs805136
Biobankrs805136
1000 genomesrs805136
hgdprs805136
ensemblrs805136
geneviewrs805136
scholarrs805136
googlers805136
pharmgkbrs805136
gwascentralrs805136
openSNPrs805136
23andMers805136
SNPshotrs805136
SNPdbers805136
MSV3drs805136
GWAS Ctlgrs805136
Max Magnitude0

[PMID 20057365] Meta-analysis added power to identify variants in FTO associated with type 2 diabetes and obesity in the Asian population [PMID 20502638OA-icon.png] Risk of type 2 diabetes and obesity is differentially associated with variation in FTO in whites and African-Americans in the ARIC study.

[PMID 23136261OA-icon.png] Fat mass and obesity gene and cognitive decline: The Atherosclerosis Risk in Communities Study