Variant (rsID / SNP)
rs1944270
rs1944270 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SERPINB8. Location: chromosome 18, position 61,647,069. The table records no clinical significance for this variant.
Reference-table entries
SERPINB8Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:61647069
- HGVS
- NM_001366198.1,c.203G>A,p.Arg68Gln
- Allele change
- Missense_R68Q
Associated conditions / phenotypes
Silent|Missense_R68Q|Missense_R68Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.