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rs145433814

From SNPedia

Orientationplus
Stabilizedplus
Make rs145433814(A;A)
Make rs145433814(A;G)
Make rs145433814(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position59899176
is asnp
is mentioned by
dbSNPrs145433814
ebirs145433814
HLIrs145433814
Exacrs145433814
Varsomers145433814
Maprs145433814
PheGenIrs145433814
hapmaprs145433814
1000 genomesrs145433814
hgdprs145433814
ensemblrs145433814
gopubmedrs145433814
geneviewrs145433814
scholarrs145433814
googlers145433814
pharmgkbrs145433814
gwascentralrs145433814
openSNPrs145433814
23andMers145433814
23andMe allrs145433814
SNP Nexus

SNPshotrs145433814
SNPdbers145433814
MSV3drs145433814
GWAS Ctlgrs145433814
GMAF0.008264
Max Magnitude
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Eating disorders (purging via substances)
Title Genetic variants associated with disordered eating.
Risk Allele G
P-val 6E-6
Odds Ratio .24 [0.14-0.34] unit decrease