Variant (rsID / SNP)
rs2302190
rs2302190 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTMR4. Location: chromosome 17, position 56,584,508. The table records no clinical significance for this variant.
Reference-table entries
MTMR4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:56584508
- HGVS
- NM_001378067.1,c.880A>G,p.Ser294Gly
- Allele change
- Missense_S280G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.