Variant (rsID / SNP)
rs1050631
rs1050631 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC39A6. Location: chromosome 18, position 33,694,120. The table records no clinical significance for this variant.
Reference-table entries
SLC39A6Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 18:33694120
- HGVS
- NM_012319.4,c.1783C>T,p.Leu595Leu
- Allele change
- Synonymous_L595L
Associated conditions / phenotypes
Gastric Adenocarcinoma|Adenocarcinoma|Esophageal Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.