Variant (rsID / SNP)

rs2481

rs2481 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYH9. Location: chromosome 22, position 36,677,400. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MYH9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:36677400
Cytoband: 22q12.3
HGVS: NM_002473.6(MYH9):c.*1314C>T
Allele change: Silent

Associated conditions / phenotypes

MYH9-related disorder|Autosomal dominant nonsyndromic hearing loss 17

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.