Variant (rsID / SNP)
rs3735642
rs3735642 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCC1. Location: chromosome 7, position 127,224,286. The table records no clinical significance for this variant.
Reference-table entries
GCC1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:127224286
- HGVS
- NM_024523.6,c.951T>C,p.Asp317Asp
- Allele change
- Synonymous_D317D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.