Variant (rsID / SNP)
rs35739383
rs35739383 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTCL1. Location: chromosome 18, position 8,783,835. The table records no clinical significance for this variant.
Reference-table entries
MTCL1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:8783835
- HGVS
- NM_001395333.1,c.1805T>C,p.Met602Thr
- Allele change
- Missense_M242T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.