Variant (rsID / SNP)

rs1371932

rs1371932 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMPRSS11A. Location: chromosome 4, position 68,780,399. The table records no clinical significance for this variant.

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Reference-table entries

TMPRSS11ANot classified

Variant type: synonymous_variant
Chromosome / position: 4:68780399
HGVS: NM_182606.4,c.1011T>C,p.Asp337Asp
Allele change: Synonymous_D334D

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.