Variant (rsID / SNP)
rs9416746
rs9416746 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BICC1. Location: chromosome 10, position 60,573,753. The table records no clinical significance for this variant.
Reference-table entries
BICC1Not classified
- Variant type
- splice_region_variant&intron_variant
- Chromosome / position
- 10:60573753
- HGVS
- NM_001080512.3,c.2533+7G>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.