rs10781499

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs10781499(A;A)

Make rs10781499(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

136371953

Gene

CARD9

is a	snp
is	mentioned by
dbSNP	rs10781499
dbSNP (classic)	rs10781499
ClinGen	rs10781499
ebi	rs10781499
HLI	rs10781499
Exac	rs10781499
Gnomad	rs10781499
Varsome	rs10781499
LitVar	rs10781499
Map	rs10781499
PheGenI	rs10781499
Biobank	rs10781499
1000 genomes	rs10781499
hgdp	rs10781499
ensembl	rs10781499
geneview	rs10781499
scholar	rs10781499
google	rs10781499
pharmgkb	rs10781499
gwascentral	rs10781499
openSNP	rs10781499
23andMe	rs10781499
SNPshot	rs10781499
SNPdbe	rs10781499
MSV3d	rs10781499
GWAS Ctlg	rs10781499

GMAF

0.365

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21297633]
Trait
Title	Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Risk Allele	A
P-val	3E-19
Odds Ratio	1.1200 [1.08-1.17]

GWAS snp
PMID	[PMID 23128233]
Trait	Inflammatory bowel disease
Title	Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele	A
P-val	4E-56
Odds Ratio	1.19 [1.154-1.222]

ClinVar
Risk	rs10781499(A;A)
Alt	rs10781499(A;A)
Reference	Rs10781499(G;G)
Significance	Non-pathogenic
Disease	Familial Candidiasis not specified
Variation	info
Gene	CARD9 DNLZ
CLNDBN	Familial Candidiasis, Recessive not specified
Reversed	0
HGVS	NC_000009.11:g.139266405G>A
CLNSRC
CLNACC	RCV000351119.1, RCV000455755.1,