Variant (rsID / SNP)

rs445520

rs445520 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC11A2. Location: chromosome 12, position 51,402,905. The table records no clinical significance for this variant.

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Reference-table entries

SLC11A2Not classified

Variant type: missense_variant
Chromosome / position: 12:51402905
HGVS: NM_001379448.1,c.17A>C,p.Tyr6Ser
Allele change: Silent

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.