Variant (rsID / SNP)

rs149411

rs149411 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC11A2. Location: chromosome 12, position 51,380,232. Clinical significance in the table: Benign.

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Reference-table entries

SLC11A2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:51380232
Cytoband: 12q13.12
HGVS: NM_000617.3(SLC11A2):c.*1876T>C
Allele change: Silent

Associated conditions / phenotypes

Microcytic anemia with liver iron overload

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.