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rs1545620

From SNPedia

Orientationminus
Stabilizedminus
Make rs1545620(A;A)
Make rs1545620(A;C)
Make rs1545620(C;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position17192965
GeneMYO9B
is asnp
is mentioned by
dbSNPrs1545620
ebirs1545620
HLIrs1545620
Exacrs1545620
Varsomers1545620
Maprs1545620
PheGenIrs1545620
hapmaprs1545620
1000 genomesrs1545620
hgdprs1545620
ensemblrs1545620
gopubmedrs1545620
geneviewrs1545620
scholarrs1545620
googlers1545620
pharmgkbrs1545620
gwascentralrs1545620
openSNPrs1545620
23andMers1545620
23andMe allrs1545620
SNP Nexus

SNPshotrs1545620
SNPdbers1545620
MSV3drs1545620
GWAS Ctlgrs1545620
GMAF0.3774
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 21648020] Haplotype-based analysis of ulcerative colitis risk loci identifies both IL2 and IL21 as susceptibility genes in Han Chinese


[PMID 17087940] Genetic variation in myosin IXB is associated with ulcerative colitis.


[PMID 17667713] Analysis of candidate genes on chromosomes 5q and 19p in celiac disease.


[PMID 17944996] The association of MYO9B gene in Italian patients with inflammatory bowel diseases.


[PMID 19142207OA-icon.png] MYO9B polymorphisms in multiple sclerosis.


[PMID 19235913] Association between genetic variants in myosin IXB and Crohn's disease.


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


[PMID 21515326] Replication of genetic variation in the MYO9B gene in Crohn's disease.


GET Evidence
MYO9B-S1011A
aa_change Ser1011Ala
aa_change_short S1011A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.530502
summary



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