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rs17496827

From SNPedia

Orientationplus
Stabilizedplus
Make rs17496827(A;A)
Make rs17496827(A;C)
Make rs17496827(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position222488727
GeneSGPP2
is asnp
is mentioned by
dbSNPrs17496827
ebirs17496827
HLIrs17496827
Exacrs17496827
Varsomers17496827
Maprs17496827
PheGenIrs17496827
hapmaprs17496827
1000 genomesrs17496827
hgdprs17496827
ensemblrs17496827
gopubmedrs17496827
geneviewrs17496827
scholarrs17496827
googlers17496827
pharmgkbrs17496827
gwascentralrs17496827
openSNPrs17496827
23andMers17496827
23andMe allrs17496827
SNP Nexus

SNPshotrs17496827
SNPdbers17496827
MSV3drs17496827
GWAS Ctlgrs17496827
GMAF0.4803
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Anorexia nervosa
Title Genetic variants associated with disordered eating.
Risk Allele C
P-val 7E-6
Odds Ratio .04 [0.024-0.06] unit decrease