Variant (rsID / SNP)
rs1042058
rs1042058 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAP3K8. Location: chromosome 10, position 30,728,101. The table records no clinical significance for this variant.
Reference-table entries
MAP3K8Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 10:30728101
- HGVS
- NM_001244134.1,c.234T>C,p.Tyr78Tyr
- Allele change
- Synonymous_Y78Y
Associated conditions / phenotypes
Crohn's Disease|Inflammatory Bowel Disease|Ulcerative Colitis|Cytokine Deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.