Variant (rsID / SNP)

rs111033537

rs111033537 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMPRSS3. Location: chromosome 21, position 43,796,661. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TMPRSS3Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 21:43796661
Cytoband: 21q22.3
HGVS: NM_001256317.3(TMPRSS3):c.1180G>C (p.Asp394His)
Allele change: Missense_D394H

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.