Variant (rsID / SNP)
rs896378
rs896378 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC39A14. Location: chromosome 8, position 22,262,321. The table records no clinical significance for this variant.
Reference-table entries
SLC39A14Not classified
- Variant type
- missense_variant
- Chromosome / position
- 8:22262321
- HGVS
- NM_001351657.2,c.128T>C,p.Leu43Pro
- Allele change
- Missense_L43P
Associated conditions / phenotypes
Missense_L33P|Missense_L33P|Missense_L33P|Missense_L43P|Missense_L33P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.