Variant (rsID / SNP)
rs1047626
rs1047626 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC30A9. Location: chromosome 4, position 42,003,671. The table records no clinical significance for this variant.
Reference-table entries
SLC30A9Not classified
- Variant type
- missense_variant
- Chromosome / position
- 4:42003671
- HGVS
- NM_006345.4,c.148A>G,p.Met50Val
- Allele change
- Missense_M50V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.