Variant (rsID / SNP)
rs666623
rs666623 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGDCC3. Location: chromosome 15, position 65,667,724. The table records no clinical significance for this variant.
Reference-table entries
IGDCC3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 15:65667724
- HGVS
- NM_004884.4,c.120T>C,p.Ala40Ala
- Allele change
- Synonymous_A40A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.