Variant (rsID / SNP)
rs61735130
rs61735130 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASB10. Location: chromosome 7, position 150,878,220. Clinical significance in the table: Benign.
Reference-table entries
ASB10Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:150878220
- Cytoband
- 7q36.1
- HGVS
- NM_001142459.2(ASB10):c.910C>T (p.Arg304Cys)
- Allele change
- Missense_R304C
Associated conditions / phenotypes
Glaucoma 1, open angle, F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.