Variant (rsID / SNP)
rs72811487
rs72811487 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIEZO1. Location: chromosome 16, position 88,788,060. Clinical significance in the table: Benign.
Reference-table entries
PIEZO1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- synonymous_variant
- Chromosome / position
- 16:88788060
- HGVS
- NM_001142864.4,c.5289C>T,p.Tyr1763Tyr
- Allele change
- Synonymous_Y1763Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.