Variant (rsID / SNP)
rs1650697
rs1650697 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH3, DHFR. Location: chromosome 5, position 79,950,781. Clinical significance in the table: Benign.
Reference-table entries
MSH3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:79950781
- Cytoband
- 5q14.1
- HGVS
- NM_000791.4(DHFR):c.-473T>C
- Allele change
- Silent
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Constitutional megaloblastic anemia with severe neurologic disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.