Variant (rsID / SNP)
rs79077926
rs79077926 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PROM1. Location: chromosome 4, position 15,993,857. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
PROM1Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:15993857
- Cytoband
- 4p15.32
- HGVS
- NM_006017.3(PROM1):c.1911+14G>A
- Allele change
- Silent
Associated conditions / phenotypes
Stargardt disease 4|Retinal macular dystrophy type 2|Cone-rod dystrophy 12|Retinitis pigmentosa
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.