Variant (rsID / SNP)

rs73038753

rs73038753 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CRX. Location: chromosome 19, position 48,345,241. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CRXBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:48345241
Cytoband: 19q13.33
HGVS: NM_000554.6(CRX):c.*2017C>T
Allele change: Silent

Associated conditions / phenotypes

Leber congenital amaurosis 7|Cone-rod dystrophy 2|Retinitis pigmentosa

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.