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rs1056513

From SNPedia

Orientationplus
Stabilizedplus
Make rs1056513(A;A)
Make rs1056513(A;G)
Make rs1056513(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position61914626
GeneINADL
is asnp
is mentioned by
dbSNPrs1056513
ebirs1056513
HLIrs1056513
Exacrs1056513
Varsomers1056513
Maprs1056513
PheGenIrs1056513
hapmaprs1056513
1000 genomesrs1056513
hgdprs1056513
ensemblrs1056513
gopubmedrs1056513
geneviewrs1056513
scholarrs1056513
googlers1056513
pharmgkbrs1056513
gwascentralrs1056513
openSNPrs1056513
23andMers1056513
23andMe allrs1056513
SNP Nexus

SNPshotrs1056513
SNPdbers1056513
MSV3drs1056513
GWAS Ctlgrs1056513
GMAF0.4862
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 23251661OA-icon.png] Novel genetic Loci identified for the pathophysiology of childhood obesity in the Hispanic population