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rs10744391

From SNPedia

Orientationplus
Stabilizedplus
Make rs10744391(A;A)
Make rs10744391(A;G)
Make rs10744391(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position128840393
is asnp
is mentioned by
dbSNPrs10744391
ebirs10744391
HLIrs10744391
Exacrs10744391
Varsomers10744391
Maprs10744391
PheGenIrs10744391
hapmaprs10744391
1000 genomesrs10744391
hgdprs10744391
ensemblrs10744391
gopubmedrs10744391
geneviewrs10744391
scholarrs10744391
googlers10744391
pharmgkbrs10744391
gwascentralrs10744391
openSNPrs10744391
23andMers10744391
23andMe allrs10744391
SNP Nexus

SNPshotrs10744391
SNPdbers10744391
MSV3drs10744391
GWAS Ctlgrs10744391
GMAF0.2511
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22044751OA-icon.png]
Trait
Title Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.
Risk Allele A
P-val 0.000001
Odds Ratio 0.2240 None