Variant (rsID / SNP)

rs117385282

rs117385282 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RSPH1. Location: chromosome 21, position 43,896,143. Clinical significance in the table: Benign.

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Reference-table entries

RSPH1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 21:43896143
Cytoband: 21q22.3
HGVS: NM_080860.4(RSPH1):c.742G>A (p.Gly248Arg)
Allele change: Missense_G248R

Associated conditions / phenotypes

Primary ciliary dyskinesia|Primary ciliary dyskinesia 24

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.