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rs12785341

From SNPedia

Orientationplus
Stabilizedplus
Make rs12785341(A;A)
Make rs12785341(A;C)
Make rs12785341(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position110525134
is asnp
is mentioned by
dbSNPrs12785341
ebirs12785341
HLIrs12785341
Exacrs12785341
Varsomers12785341
Maprs12785341
PheGenIrs12785341
hapmaprs12785341
1000 genomesrs12785341
hgdprs12785341
ensemblrs12785341
gopubmedrs12785341
geneviewrs12785341
scholarrs12785341
googlers12785341
pharmgkbrs12785341
gwascentralrs12785341
openSNPrs12785341
23andMers12785341
23andMe allrs12785341
SNP Nexus

SNPshotrs12785341
SNPdbers12785341
MSV3drs12785341
GWAS Ctlgrs12785341
GMAF0.06657
Max Magnitude
? (A;A) (A;C) (C;C) 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 C
P-val 0.000008
Odds Ratio 0.2900 None