Variant (rsID / SNP)
rs11077986
rs11077986 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SECTM1. Location: chromosome 17, position 80,280,865. The table records no clinical significance for this variant.
Reference-table entries
SECTM1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:80280865
- HGVS
- NM_003004.3,c.426C>T,p.Pro142Pro
- Allele change
- Synonymous_P142P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.