Variant (rsID / SNP)

rs869312085

rs869312085 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTN. Location: chromosome 2, position 179,404,286. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

TTNLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 2:179404286
Cytoband: 2q31.2
HGVS: NM_001267550.2(TTN):c.98506C>T (p.Arg32836Ter)
Allele change: Silent

Associated conditions / phenotypes

Primary dilated cardiomyopathy|Cardiovascular phenotype|Dilated cardiomyopathy 1G|Autosomal recessive limb-girdle muscular dystrophy type 2J|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.