Variant (rsID / SNP)

rs12614435

rs12614435 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTN. Location: chromosome 2, position 179,489,726. Clinical significance in the table: Benign.

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Reference-table entries

TTNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:179489726
Cytoband: 2q31.2
HGVS: NM_001267550.2(TTN):c.44549-268T>C
Allele change: Silent

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.