Variant (rsID / SNP)

rs10798333

rs10798333 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNN. Location: chromosome 1, position 175,092,707. The table records no clinical significance for this variant.

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Reference-table entries

TNNNot classified

Variant type: missense_variant
Chromosome / position: 1:175092707
HGVS: NM_022093.2,c.2822C>T,p.Thr941Met
Allele change: Missense_T941M

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.