Variant (rsID / SNP)

rs6927567

rs6927567 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RSPH4A. Location: chromosome 6, position 116,950,734. Clinical significance in the table: Benign.

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Reference-table entries

RSPH4ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:116950734
Cytoband: 6q22.1
HGVS: NM_001010892.3(RSPH4A):c.1667G>A (p.Arg556His)
Allele change: Missense_R556H

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.