rs10512734

Orientation

plus

Stabilized

plus

Make rs10512734(A;A)

Make rs10512734(A;G)

Make rs10512734(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

40393503

is a	snp
is	mentioned by
dbSNP	rs10512734
dbSNP (classic)	rs10512734
ClinGen	rs10512734
ebi	rs10512734
HLI	rs10512734
Exac	rs10512734
Gnomad	rs10512734
Varsome	rs10512734
LitVar	rs10512734
Map	rs10512734
PheGenI	rs10512734
Biobank	rs10512734
1000 genomes	rs10512734
hgdp	rs10512734
ensembl	rs10512734
geneview	rs10512734
scholar	rs10512734
google	rs10512734
pharmgkb	rs10512734
gwascentral	rs10512734
openSNP	rs10512734
23andMe	rs10512734
SNPshot	rs10512734
SNPdbe	rs10512734
MSV3d	rs10512734
GWAS Ctlg	rs10512734

GMAF

0.4017

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

Rs10512734
PubMed	[PMID 17447842]
Affy Probeset	SNP_A-4264861
Affy Orientation	reverse
On GW 5.0	1
Alleles A/B	C/T
Ancestral	G
Population	EU
Allele	A
Case Freq.	0.76
Control Freq.	0.67
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All	1.63
Disease	Crohn's disease (CD)

rs10512734 increases susceptibility to Crohn's disease 1.63 times for carriers of the A allele [PMID 17447842]