Variant (rsID / SNP)
rs7792760
rs7792760 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYO1G. Location: chromosome 7, position 45,004,063. The table records no clinical significance for this variant.
Reference-table entries
MYO1GNot classified
- Variant type
- missense_variant
- Chromosome / position
- 7:45004063
- HGVS
- NM_033054.3,c.2582A>G,p.Gln861Arg
- Allele change
- Missense_Q861R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.