Variant (rsID / SNP)
rs10033189
rs10033189 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PROM1. Location: chromosome 4, position 16,077,515. Clinical significance in the table: Benign.
Reference-table entries
PROM1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:16077515
- Cytoband
- 4p15.32
- HGVS
- NM_006017.3(PROM1):c.15C>T (p.Leu5=)
- Allele change
- Synonymous_L5L
Associated conditions / phenotypes
Stargardt disease 4|Cone-rod dystrophy 12|Retinal macular dystrophy type 2|Retinitis pigmentosa
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.