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rs76765968

From SNPedia

Orientationplus
Stabilizedplus
Make rs76765968(C;C)
Make rs76765968(C;T)
Make rs76765968(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position85934535
GeneGRID1
is asnp
is mentioned by
dbSNPrs76765968
ebirs76765968
HLIrs76765968
Exacrs76765968
Varsomers76765968
Maprs76765968
PheGenIrs76765968
hapmaprs76765968
1000 genomesrs76765968
hgdprs76765968
ensemblrs76765968
gopubmedrs76765968
geneviewrs76765968
scholarrs76765968
googlers76765968
pharmgkbrs76765968
gwascentralrs76765968
openSNPrs76765968
23andMers76765968
23andMe allrs76765968
SNP Nexus

SNPshotrs76765968
SNPdbers76765968
MSV3drs76765968
GWAS Ctlgrs76765968
GMAF0.07805
Max Magnitude
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Anorexia nervosa
Title Genetic variants associated with disordered eating.
Risk Allele T
P-val 2E-6
Odds Ratio .06 [0.037-0.091] unit decrease