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rs1048466

From SNPedia

Orientationplus
Stabilizedplus
Make rs1048466(A;A)
Make rs1048466(A;G)
Make rs1048466(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position442384
GeneCCDC77
is asnp
is mentioned by
dbSNPrs1048466
ebirs1048466
HLIrs1048466
Exacrs1048466
Varsomers1048466
Maprs1048466
PheGenIrs1048466
hapmaprs1048466
1000 genomesrs1048466
hgdprs1048466
ensemblrs1048466
gopubmedrs1048466
geneviewrs1048466
scholarrs1048466
googlers1048466
pharmgkbrs1048466
gwascentralrs1048466
openSNPrs1048466
23andMers1048466
23andMe allrs1048466
SNP Nexus

SNPshotrs1048466
SNPdbers1048466
MSV3drs1048466
GWAS Ctlgrs1048466
GMAF0.242
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23563609OA-icon.png]
Trait Obesity (early onset extreme)
Title Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
Risk Allele G
P-val 8E-8
Odds Ratio 1.22 [1.14-1.32]