Variant (rsID / SNP)
rs310586
rs310586 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IQCA1L. Location: chromosome 7, position 150,893,629. The table records no clinical significance for this variant.
Reference-table entries
IQCA1LNot classified
- Variant type
- missense_variant
- Chromosome / position
- 7:150893629
- HGVS
- NM_001304419.2,c.1219A>G,p.Asn407Asp
- Allele change
- Missense_N407D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.