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Variant (rsID / SNP)

rs41302239

USH2A

rs41302239 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USH2A. Location: chromosome 1, position 216,243,634. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

USH2AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:216243634
Cytoband
1q41
HGVS
NM_206933.4(USH2A):c.5858C>G (p.Ala1953Gly)
Allele change
Missense_A1953G

Associated conditions / phenotypes

Retinal dystrophy|Retinitis pigmentosa 39|Usher syndrome type 2A|Usher syndrome type 2A|Retinitis pigmentosa 39

Public references

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