Variant (rsID / SNP)
rs760915898
rs760915898 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP290. Location: chromosome 12, position 88,479,815. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
CEP290Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:88479815
- Cytoband
- 12q21.32
- HGVS
- NM_025114.4(CEP290):c.4437+1G>A
- Allele change
- Silent
Associated conditions / phenotypes
Nephronophthisis|Joubert syndrome|Meckel-Gruber syndrome|Joubert syndrome 5|Bardet-Biedl syndrome 14|Leber congenital amaurosis 10|Meckel syndrome, type 4|Senior-Loken syndrome 6|CEP290-Related Disorders|Leber congenital amaurosis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.