Variant (rsID / SNP)

rs104894878

rs104894878 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDP. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

NDPPathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Cytoband: Xp11.3
HGVS: NM_000266.4(NDP):c.361C>T (p.Arg121Trp)
Allele change: Missense_R121W

Associated conditions / phenotypes

Exudative vitreoretinopathy 2, X-linked

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.