rs2006996

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs2006996(C;C)

Make rs2006996(C;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

114830358

is a	snp
is	mentioned by
dbSNP	rs2006996
dbSNP (classic)	rs2006996
ClinGen	rs2006996
ebi	rs2006996
HLI	rs2006996
Exac	rs2006996
Gnomad	rs2006996
Varsome	rs2006996
LitVar	rs2006996
Map	rs2006996
PheGenI	rs2006996
Biobank	rs2006996
1000 genomes	rs2006996
hgdp	rs2006996
ensembl	rs2006996
geneview	rs2006996
scholar	rs2006996
google	rs2006996
pharmgkb	rs2006996
gwascentral	rs2006996
openSNP	rs2006996
23andMe	rs2006996
SNPshot	rs2006996
SNPdbe	rs2006996
MSV3d	rs2006996
GWAS Ctlg	rs2006996

GMAF

0.141

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 21699788]
Trait
Title	HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease.
Risk Allele	T
P-val	4E-13
Odds Ratio	1.6700 [1.47-1.92]