Variant (rsID / SNP)

rs62638629

rs62638629 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RPGR. The table records no clinical significance for this variant.

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Reference-table entries

RPGRNot classified

Variant type: single nucleotide variant
Cytoband: Xp11.4
HGVS: NM_001034853.2(RPGR):c.127G>A (p.Gly43Arg)
Allele change: Missense_G43R

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.