Variant (rsID / SNP)

rs2478568

rs2478568 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC39A12. Location: chromosome 10, position 18,266,989. The table records no clinical significance for this variant.

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Reference-table entries

SLC39A12Not classified

Variant type: missense_variant
Chromosome / position: 10:18266989
HGVS: NM_001145195.2,c.910G>A,p.Val304Ile
Allele change: Missense_V170I

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.