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Variant (rsID / SNP)

rs375447438

TNNI3

rs375447438 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNI3. Location: chromosome 19, position 55,663,167. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TNNI3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
19:55663167
Cytoband
19q13.42
HGVS
NM_000363.5(TNNI3):c.*35C>T
Allele change
Silent

Associated conditions / phenotypes

Dilated cardiomyopathy 2A|Hypertrophic cardiomyopathy 7|Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome|Cardiomyopathy, familial restrictive, 1

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.