Variant (rsID / SNP)
rs61756687
rs61756687 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHIA. Location: chromosome 1, position 111,857,951. The table records no clinical significance for this variant.
Reference-table entries
CHIANot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:111857951
- HGVS
- NM_201653.4,c.374A>G,p.Lys125Arg
- Allele change
- Silent
Associated conditions / phenotypes
Eumycotic Mycetoma|Mycetoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.