Variant (rsID / SNP)

rs397516346

rs397516346 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNI3. Location: chromosome 19, position 55,668,487. Clinical significance in the table: Likely benign.

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Reference-table entries

TNNI3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:55668487
Cytoband: 19q13.42
HGVS: NM_000363.5(TNNI3):c.39C>G (p.Arg13=)
Allele change: Missense_A13G

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.