Variant (rsID / SNP)
rs344141
rs344141 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SHROOM3. Location: chromosome 4, position 77,660,731. Clinical significance in the table: Benign.
Reference-table entries
SHROOM3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:77660731
- Cytoband
- 4q21.1
- HGVS
- NM_020859.4(SHROOM3):c.1405C>G (p.Pro469Ala)
- Allele change
- Missense_P469A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.