Variant (rsID / SNP)
rs4741289
rs4741289 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MPDZ. Location: chromosome 9, position 13,190,163. Clinical significance in the table: Benign.
Reference-table entries
MPDZBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:13190163
- Cytoband
- 9p23
- HGVS
- NM_001378778.1(MPDZ):c.2104G>A (p.Glu702Lys)
- Allele change
- Missense_E702K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.