Variant (rsID / SNP)

rs28362592

rs28362592 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNT1. Location: chromosome 19, position 55,660,499. Clinical significance in the table: Benign.

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Reference-table entries

TNNT1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:55660499
Cytoband: 19q13.42
HGVS: NM_003283.6(TNNT1):c.-12+30T>C
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.