Variant (rsID / SNP)
rs3825393
rs3825393 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO1H. Location: chromosome 12, position 109,883,374. The table records no clinical significance for this variant.
Reference-table entries
MYO1HNot classified
- Variant type
- missense_variant
- Chromosome / position
- 12:109883374
- HGVS
- NM_001101421.4,c.3050T>C,p.Leu1017Pro
- Allele change
- Missense_L1001P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.