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rs2305767

From SNPedia

Orientationminus
Stabilizedminus
Make rs2305767(A;A)
Make rs2305767(A;G)
Make rs2305767(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position17183487
GeneMYO9B
is asnp
is mentioned by
dbSNPrs2305767
ebirs2305767
HLIrs2305767
Exacrs2305767
Varsomers2305767
Maprs2305767
PheGenIrs2305767
hapmaprs2305767
1000 genomesrs2305767
hgdprs2305767
ensemblrs2305767
gopubmedrs2305767
geneviewrs2305767
scholarrs2305767
googlers2305767
pharmgkbrs2305767
gwascentralrs2305767
openSNPrs2305767
23andMers2305767
23andMe allrs2305767
SNP Nexus

SNPshotrs2305767
SNPdbers2305767
MSV3drs2305767
GWAS Ctlgrs2305767
GMAF0.253
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 17948900] rs2305767 (P = 1.16 x 10(-4); OR 1.41, 95% CI 1.18-1.67). We demonstrate significant association of allelic variants in MYO9B with schizophrenia

[PMID 19235913] Crohn's disease rs2305767 associated with inflammatory bowel disease (IBD) overall (corrected P-value 0.002, odds ratio [OR] 0.76, 95% confidence interval [CI] 0.67-0.86)

However, a 2016 meta-analysis including 8 studies (totaling 2272 cases and 5419 controls) found no significant association for this SNP and celiac disease in Caucasian populations.[PMID 27219348]


[PMID 17176439] No evidence of association of the MYO9B polymorphisms with celiac disease in the Spanish population.


[PMID 17584584] MYO9B gene polymorphisms are associated with autoimmune diseases in Spanish population.


[PMID 20303373] Association analysis of myosin IXB and type 1 diabetes.


[PMID 23368647] Frequency of MYO9B polymorphisms in celiac patients and controls


[PMID 27556856] MYO9B gene polymorphisms are associated with the risk of inflammatory bowel diseases.