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rs10494067

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs10494067(A;C)
Make rs10494067(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position107288236
GeneNTNG1
is asnp
is mentioned by
dbSNPrs10494067
ebirs10494067
HLIrs10494067
Exacrs10494067
Varsomers10494067
Maprs10494067
PheGenIrs10494067
hapmaprs10494067
1000 genomesrs10494067
hgdprs10494067
ensemblrs10494067
gopubmedrs10494067
geneviewrs10494067
scholarrs10494067
googlers10494067
pharmgkbrs10494067
gwascentralrs10494067
openSNPrs10494067
23andMers10494067
23andMe allrs10494067
SNP Nexus

SNPshotrs10494067
SNPdbers10494067
MSV3drs10494067
GWAS Ctlgrs10494067
GMAF0.04821
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21079607OA-icon.png]
Trait
Title A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa
Risk Allele
P-val 0.000006
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.