Variant (rsID / SNP)

rs41313732

rs41313732 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USH2A. Location: chromosome 1, position 216,465,626. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

USH2ABenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:216465626
Cytoband: 1q41
HGVS: NM_206933.4(USH2A):c.1731C>T (p.Cys577=)
Allele change: Synonymous_C577C

Associated conditions / phenotypes

Usher syndrome type 2A|Retinitis pigmentosa

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.