Variant (rsID / SNP)
rs4948550
rs4948550 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BICC1. Location: chromosome 10, position 60,588,553. The table records no clinical significance for this variant.
Reference-table entries
BICC1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:60588553
- HGVS
- NM_001080512.3,c.2827T>C,p.Ser943Pro
- Allele change
- Missense_S943P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.