Variant (rsID / SNP)

rs10030708

rs10030708 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMPRSS11F. Location: chromosome 4, position 68,995,529. The table records no clinical significance for this variant.

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Reference-table entries

TMPRSS11FNot classified

Variant type: missense_variant&splice_region_variant
Chromosome / position: 4:68995529
HGVS: NM_207407.2,c.10G>A,p.Ala4Thr
Allele change: Missense_A4T

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.