Variant (rsID / SNP)

rs17032000

rs17032000 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRAT. Location: chromosome 4, position 155,672,958. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

LRATBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:155672958
Cytoband: 4q32.1
HGVS: NM_004744.5(LRAT):c.*2670G>T
Allele change: Silent

Associated conditions / phenotypes

Retinitis pigmentosa|Leber congenital amaurosis|Leber congenital amaurosis 14

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.