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rs148915469

From SNPedia

Orientationplus
Stabilizedplus
Make rs148915469(A;A)
Make rs148915469(A;C)
Make rs148915469(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position99474257
is asnp
is mentioned by
dbSNPrs148915469
dbSNP (old)rs148915469
ClinGenrs148915469
ebirs148915469
HLIrs148915469
Exacrs148915469
Gnomadrs148915469
Varsomers148915469
Maprs148915469
PheGenIrs148915469
Biobankrs148915469
1000 genomesrs148915469
hgdprs148915469
ensemblrs148915469
gopubmedrs148915469
geneviewrs148915469
scholarrs148915469
googlers148915469
pharmgkbrs148915469
gwascentralrs148915469
openSNPrs148915469
23andMers148915469
23andMe allrs148915469
SNP Nexus

SNPshotrs148915469
SNPdbers148915469
MSV3drs148915469
GWAS Ctlgrs148915469
GMAF0.01928
Max Magnitude
GWAS snp
PMID [PMID 23568457OA-icon.png]
Trait Eating disorders
Title Genetic variants associated with disordered eating.
Risk Allele C
P-val 8E-6
Odds Ratio .28 [0.16-0.4] unit decrease