Variant (rsID / SNP)

rs754273

rs754273 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH6. Location: chromosome 2, position 85,023,554. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DNAH6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:85023554
Cytoband: 2p11.2
HGVS: NM_001370.2(DNAH6):c.11359+5A>G
Allele change: Silent

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.