Variant (rsID / SNP)

rs368781863

rs368781863 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTN. Location: chromosome 2, position 179,537,372. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TTNBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:179537372
Cytoband: 2q31.2
HGVS: NM_001267550.2(TTN):c.34845C>T (p.Pro11615=)
Allele change: Silent

Associated conditions / phenotypes

Dilated cardiomyopathy 1G|Autosomal recessive limb-girdle muscular dystrophy type 2J

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.