Variant (rsID / SNP)
rs2612086
rs2612086 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ENOSF1. Location: chromosome 18, position 691,266. The table records no clinical significance for this variant.
Reference-table entries
ENOSF1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:691266
- HGVS
- NM_001354067.2,c.578T>C,p.Met193Thr
- Allele change
- Silent
Associated conditions / phenotypes
Missense_M193T|Missense_M145T|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.