rs1506203

Orientation

minus

Stabilized

minus

Make rs1506203(A;A)

Make rs1506203(A;C)

Make rs1506203(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

30999011

is a	snp
is	mentioned by
dbSNP	rs1506203
dbSNP (classic)	rs1506203
ClinGen	rs1506203
ebi	rs1506203
HLI	rs1506203
Exac	rs1506203
Gnomad	rs1506203
Varsome	rs1506203
LitVar	rs1506203
Map	rs1506203
PheGenI	rs1506203
Biobank	rs1506203
1000 genomes	rs1506203
hgdp	rs1506203
ensembl	rs1506203
geneview	rs1506203
scholar	rs1506203
google	rs1506203
pharmgkb	rs1506203
gwascentral	rs1506203
openSNP	rs1506203
23andMe	rs1506203
SNPshot	rs1506203
SNPdbe	rs1506203
MSV3d	rs1506203
GWAS Ctlg	rs1506203

GMAF

0.1933

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

GWAS snp
PMID	[PMID 23568457]
Trait	Eating disorders (purging via substances)
Title	Genetic variants associated with disordered eating.
Risk Allele	G
P-val	8E-6
Odds Ratio	.08 [0.048-0.118] unit decrease