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rs13077017

From SNPedia

Orientationplus
Stabilizedplus
Make rs13077017(C;C)
Make rs13077017(C;T)
Make rs13077017(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position58120049
GeneFLNB
is asnp
is mentioned by
dbSNPrs13077017
dbSNP (old)rs13077017
ClinGenrs13077017
ebirs13077017
HLIrs13077017
Exacrs13077017
Gnomadrs13077017
Varsomers13077017
Maprs13077017
PheGenIrs13077017
Biobankrs13077017
1000 genomesrs13077017
hgdprs13077017
ensemblrs13077017
gopubmedrs13077017
geneviewrs13077017
scholarrs13077017
googlers13077017
pharmgkbrs13077017
gwascentralrs13077017
openSNPrs13077017
23andMers13077017
23andMe allrs13077017
SNP Nexus

SNPshotrs13077017
SNPdbers13077017
MSV3drs13077017
GWAS Ctlgrs13077017
GMAF0.1474
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Eating disorders (purging via substances)
Title Genetic variants associated with disordered eating.
Risk Allele C
P-val 1E-6
Odds Ratio .07 [0.044-0.102] unit decrease