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rs7624327

From SNPedia

Orientationplus
Stabilizedplus
Make rs7624327(A;A)
Make rs7624327(A;G)
Make rs7624327(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position157119117
GeneLINC00880
is asnp
is mentioned by
dbSNPrs7624327
dbSNP (classic)rs7624327
ClinGenrs7624327
ebirs7624327
HLIrs7624327
Exacrs7624327
Gnomadrs7624327
Varsomers7624327
LitVarrs7624327
Maprs7624327
PheGenIrs7624327
Biobankrs7624327
1000 genomesrs7624327
hgdprs7624327
ensemblrs7624327
geneviewrs7624327
scholarrs7624327
googlers7624327
pharmgkbrs7624327
gwascentralrs7624327
openSNPrs7624327
23andMers7624327
SNPshotrs7624327
SNPdbers7624327
MSV3drs7624327
GWAS Ctlgrs7624327
GMAF0.08861
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22911880OA-icon.png]
Trait Eating disorders
Title Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.
Risk Allele A
P-val 3E-6
Odds Ratio 1.13 [1.06-1.16]