Variant (rsID / SNP)

rs2111833

rs2111833 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMPRSS6. Location: chromosome 22, position 37,480,797. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TMPRSS6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:37480797
Cytoband: 22q12.3
HGVS: NM_001374504.1(TMPRSS6):c.1056G>A (p.Ser352=)
Allele change: Synonymous_S352S

Associated conditions / phenotypes

Microcytic anemia

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.