Variant (rsID / SNP)

rs73765819

rs73765819 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RSPH4A. Location: chromosome 6, position 116,950,798. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RSPH4ABenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:116950798
Cytoband: 6q22.1
HGVS: NM_001010892.3(RSPH4A):c.1731A>G (p.Lys577=)
Allele change: Synonymous_K577K

Associated conditions / phenotypes

Primary ciliary dyskinesia|Primary ciliary dyskinesia 11

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.