Variant (rsID / SNP)
rs12386117
rs12386117 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTCL1. Location: chromosome 18, position 8,798,185. The table records no clinical significance for this variant.
Reference-table entries
MTCL1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:8798185
- HGVS
- NM_001395333.1,c.3412G>A,p.Gly1138Ser
- Allele change
- Missense_G778S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.