Variant (rsID / SNP)

rs11929695

rs11929695 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMPRSS7. Location: chromosome 3, position 111,760,773. The table records no clinical significance for this variant.

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Reference-table entries

TMPRSS7Not classified

Variant type: missense_variant
Chromosome / position: 3:111760773
HGVS: NM_001395507.1,c.305C>T,p.Thr102Ile
Allele change: Silent

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.