Variant (rsID / SNP)

rs9896398

rs9896398 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH17. Location: chromosome 17, position 76,503,593. Clinical significance in the table: Benign.

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Reference-table entries

DNAH17Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:76503593
Cytoband: 17q25.3
HGVS: NM_173628.4(DNAH17):c.4531A>G (p.Thr1511Ala)
Allele change: Missense_T1511A

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.