Variant (rsID / SNP)

rs201240150

rs201240150 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNI3. Location: chromosome 19, position 55,663,295. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TNNI3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:55663295
Cytoband: 19q13.42
HGVS: NM_000363.5(TNNI3):c.550-10C>T
Allele change: Silent

Associated conditions / phenotypes

Hypertrophic cardiomyopathy|Cardiomyopathy

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.