Variant (rsID / SNP)
rs627491
rs627491 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH14. Location: chromosome 19, position 50,813,263. Clinical significance in the table: Benign.
Reference-table entries
MYH14Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:50813263
- Cytoband
- 19q13.33
- HGVS
- NM_001145809.2(MYH14):c.*216T>G
- Allele change
- Silent
Associated conditions / phenotypes
Autosomal dominant nonsyndromic hearing loss 4A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.