Variant (rsID / SNP)

rs6965750

rs6965750 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH11. Location: chromosome 7, position 21,824,122. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

DNAH11Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:21824122
Cytoband: 7p15.3
HGVS: NM_001277115.2(DNAH11):c.9561G>A (p.Leu3187=)
Allele change: Synonymous_L3187L

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.