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rs10998035

From SNPedia

Orientationplus
Stabilizedplus
Make rs10998035(C;C)
Make rs10998035(C;T)
Make rs10998035(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position68254473
is asnp
is mentioned by
dbSNPrs10998035
ebirs10998035
HLIrs10998035
Exacrs10998035
Varsomers10998035
Maprs10998035
PheGenIrs10998035
hapmaprs10998035
1000 genomesrs10998035
hgdprs10998035
ensemblrs10998035
gopubmedrs10998035
geneviewrs10998035
scholarrs10998035
googlers10998035
pharmgkbrs10998035
gwascentralrs10998035
openSNPrs10998035
23andMers10998035
23andMe allrs10998035
SNP Nexus

SNPshotrs10998035
SNPdbers10998035
MSV3drs10998035
GWAS Ctlgrs10998035
GMAF0.1074
Max Magnitude
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 4E-6
Odds Ratio .15 [0.086-0.216] unit decrease