Variant (rsID / SNP)
rs17160563
rs17160563 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO1F. Location: chromosome 19, position 8,612,914. Clinical significance in the table: Benign.
Reference-table entries
MYO1FBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:8612914
- Cytoband
- 19p13.2
- HGVS
- NM_012335.4(MYO1F):c.1269+6C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.