Variant (rsID / SNP)

rs17025409

rs17025409 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH6. Location: chromosome 2, position 84,897,501. Clinical significance in the table: Benign.

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Reference-table entries

DNAH6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:84897501
Cytoband: 2p11.2
HGVS: NM_001370.2(DNAH6):c.6356A>G (p.Tyr2119Cys)
Allele change: Missense_Y2119C

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.