Variant (rsID / SNP)

rs397516469

rs397516469 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNT2. Location: chromosome 1, position 201,332,519. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TNNT2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:201332519
Cytoband: 1q32.1
HGVS: NM_001276345.2(TNNT2):c.505C>T (p.Arg169Ter)
Allele change: Nonsense_R159X

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.