Variant (rsID / SNP)

rs150814892

rs150814892 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH5. Location: chromosome 5, position 13,830,823. Clinical significance in the table: Likely benign.

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Reference-table entries

DNAH5Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:13830823
Cytoband: 5p15.2
HGVS: NM_001369.3(DNAH5):c.5944G>A (p.Ala1982Thr)
Allele change: Missense_A1982T

Associated conditions / phenotypes

Primary ciliary dyskinesia

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.