Variant (rsID / SNP)

rs1990236

rs1990236 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH9. Location: chromosome 17, position 11,865,462. Clinical significance in the table: Benign.

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Reference-table entries

DNAH9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:11865462
Cytoband: 17p12
HGVS: NM_001372.4(DNAH9):c.13122G>A (p.Met4374Ile)
Allele change: Missense_M4374I

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.