Variant (rsID / SNP)

rs185482276

rs185482276 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMPRSS6. Location: chromosome 22, position 37,480,861. Clinical significance in the table: Likely benign.

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Reference-table entries

TMPRSS6Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 22:37480861
Cytoband: 22q12.3
HGVS: NM_001374504.1(TMPRSS6):c.992C>T (p.Thr331Met)
Allele change: Missense_T331M

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.