Variant (rsID / SNP)
rs1545620
rs1545620 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO9B. Location: chromosome 19, position 17,303,774. The table records no clinical significance for this variant.
Reference-table entries
MYO9BNot classified
- Variant type
- missense_variant
- Chromosome / position
- 19:17303774
- HGVS
- NM_004145.4,c.3031T>G,p.Ser1011Ala
- Allele change
- Missense_S1011A
Associated conditions / phenotypes
Inflammatory Bowel Disease|Ulcerative Colitis|Crohn's Disease|Celiac Disease 1|Colitis|Ileocolitis|Acute Necrotizing Pancreatitis|Inflammatory Bowel Disease 5|Pancreatitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.