Variant (rsID / SNP)
rs922984
rs922984 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTN. Location: chromosome 2, position 179,615,887. Clinical significance in the table: Benign.
Reference-table entries
TTNBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:179615887
- Cytoband
- 2q31.2
- HGVS
- NM_133379.5(TTN):c.11240A>G (p.Asp3747Gly)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.