Variant (rsID / SNP)

rs6696455

rs6696455 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNN. Location: chromosome 1, position 175,087,729. The table records no clinical significance for this variant.

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Reference-table entries

TNNNot classified

Variant type: missense_variant
Chromosome / position: 1:175087729
HGVS: NM_022093.2,c.2419T>C,p.Trp807Arg
Allele change: Missense_W807R

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.