rs145433814

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common genotype

Make rs145433814(A;A)

Make rs145433814(A;G)

Reference

GRCh38 38.1/142

Chromosome

2

Position

59899176

is a	snp
is	mentioned by
dbSNP	rs145433814
dbSNP (classic)	rs145433814
ClinGen	rs145433814
ebi	rs145433814
HLI	rs145433814
Exac	rs145433814
Gnomad	rs145433814
Varsome	rs145433814
LitVar	rs145433814
Map	rs145433814
PheGenI	rs145433814
Biobank	rs145433814
1000 genomes	rs145433814
hgdp	rs145433814
ensembl	rs145433814
geneview	rs145433814
scholar	rs145433814
google	rs145433814
pharmgkb	rs145433814
gwascentral	rs145433814
openSNP	rs145433814
23andMe	rs145433814
SNPshot	rs145433814
SNPdbe	rs145433814
MSV3d	rs145433814
GWAS Ctlg	rs145433814

GMAF

0.008264

Max Magnitude

0

GWAS snp
PMID	[PMID 23568457]
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