Variant (rsID / SNP)
rs11612600
rs11612600 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to A2ML1. Location: chromosome 12, position 9,010,671. Clinical significance in the table: Benign.
Reference-table entries
A2ML1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:9010671
- Cytoband
- 12p13.31
- HGVS
- NM_144670.6(A2ML1):c.3237G>A (p.Val1079=)
- Allele change
- Synonymous_V1079V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.