Variant (rsID / SNP)
rs8108738
rs8108738 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAST3. Location: chromosome 19, position 18,255,359. The table records no clinical significance for this variant.
Reference-table entries
MAST3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:18255359
- HGVS
- NM_001393501.1,c.2692G>A,p.Gly898Ser
- Allele change
- Missense_G861S
Associated conditions / phenotypes
Inflammatory Bowel Disease 6
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.