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rs10175070

From SNPedia

Orientationplus
Stabilizedplus
Make rs10175070(A;A)
Make rs10175070(A;G)
Make rs10175070(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position227805859
GeneLRRC38
is asnp
is mentioned by
dbSNPrs10175070
ebirs10175070
HLIrs10175070
Exacrs10175070
Varsomers10175070
Maprs10175070
PheGenIrs10175070
hapmaprs10175070
1000 genomesrs10175070
hgdprs10175070
ensemblrs10175070
gopubmedrs10175070
geneviewrs10175070
scholarrs10175070
googlers10175070
pharmgkbrs10175070
gwascentralrs10175070
openSNPrs10175070
23andMers10175070
23andMe allrs10175070
SNP Nexus

SNPshotrs10175070
SNPdbers10175070
MSV3drs10175070
GWAS Ctlgrs10175070
GMAF0.3503
Max Magnitude
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Eating disorders (purging via substances)
Title Genetic variants associated with disordered eating.
Risk Allele A
P-val 2E-6
Odds Ratio .12 [0.073-0.175] unit increase