Annotation Detail
Information
- Associated Genes
- MYNN
- Associated Variants
-
MYNN p.His6= (p.H6=)
(
ENST00000349841.10,
ENST00000356716.8,
ENST00000544106.5 )
MYNN p.His6= (p.H6=) ( ENST00000349841.10, ENST00000356716.8, ENST00000544106.5 ) - Associated Disease
- Chronic osteomyelitis
- Source Database
- ClinVar
- Description
- NM_018657.5(MYNN):c.18C>T (p.His6=) AND Chronic osteomyelitis
- ClinVar Allele ID
- 362287
- ClinVar RefSeq Alternation Syntax
- NM_018657.5:c.18C>T
- ClinVar RefSeq Alternation Syntax
- NM_001185118.2:c.18C>T
- ClinVar RefSeq Alternation Syntax
- NM_001185119.1:c.18C>T
- ClinVar RefSeq Alternation Syntax
- NR_033702.2:n.116C>T
- ClinVar RefSeq Alternation Syntax
- NR_033703.2:n.116C>T
- Clinical Significance Description
- association
- Clinical Significance Last Update
- 2016-09-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000497621
- ClinVar Disease
- Chronic osteomyelitis
- Observed Origin Sample
- tested-inconclusive
Drugs