Variant (rsID / SNP)

rs35973257

rs35973257 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH17. Location: chromosome 17, position 76,422,599. Clinical significance in the table: Likely benign.

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Reference-table entries

DNAH17Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:76422599
Cytoband: 17q25.3
HGVS: NM_173628.4(DNAH17):c.12854G>A (p.Arg4285Gln)
Allele change: Missense_R4285Q

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.