Variant (rsID / SNP)

rs369037463

rs369037463 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RPGR. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

RPGRPathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Cytoband: Xp11.4
HGVS: NM_001034853.2(RPGR):c.505G>T (p.Glu169Ter)
Allele change: Missense_E169K

Associated conditions / phenotypes

Retinal dystrophy

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.