Variant (rsID / SNP)
rs9357283
rs9357283 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH8. Location: chromosome 6, position 38,800,164. The table records no clinical significance for this variant.
Reference-table entries
DNAH8Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:38800164
- HGVS
- NM_001206927.2,c.4255G>A,p.Glu1419Lys
- Allele change
- Missense_E1202K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
