Variant (rsID / SNP)
rs11537993
rs11537993 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRMS1. Location: chromosome 11, position 66,109,033. The table records no clinical significance for this variant.
Reference-table entries
BRMS1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:66109033
- HGVS
- NM_001024957.2,c.201A>G,p.Leu67Leu
- Allele change
- Synonymous_L67L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
