Variant (rsID / SNP)
rs2817760
rs2817760 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYPN. Location: chromosome 10, position 69,905,300. Clinical significance in the table: Benign.
Reference-table entries
MYPNBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:69905300
- Cytoband
- 10q21.3
- HGVS
- NM_032578.4(MYPN):c.1130+17G>A
- Allele change
- Silent
Associated conditions / phenotypes
Dilated cardiomyopathy 1KK
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.