Variant (rsID / SNP)

rs61744697

rs61744697 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH9. Location: chromosome 17, position 11,672,607. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DNAH9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:11672607
Cytoband: 17p12
HGVS: NM_001372.4(DNAH9):c.7513G>T (p.Val2505Leu)
Allele change: Missense_V2505L

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.