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rs17725255

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17725255(C;C)
Make rs17725255(C;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position18098487
is asnp
is mentioned by
dbSNPrs17725255
ebirs17725255
HLIrs17725255
Exacrs17725255
Varsomers17725255
Maprs17725255
PheGenIrs17725255
hapmaprs17725255
1000 genomesrs17725255
hgdprs17725255
ensemblrs17725255
gopubmedrs17725255
geneviewrs17725255
scholarrs17725255
googlers17725255
pharmgkbrs17725255
gwascentralrs17725255
openSNPrs17725255
23andMers17725255
23andMe allrs17725255
SNP Nexus

SNPshotrs17725255
SNPdbers17725255
MSV3drs17725255
GWAS Ctlgrs17725255
GMAF0.124
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21079607OA-icon.png]
Trait Anorexia nervosa
Title A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa
Risk Allele
P-val 0.000002
Odds Ratio None None

[PMID 23568457OA-icon.png] Genetic variants associated with disordered eating.

[PMID 21079607OA-icon.png] A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.