Variant (rsID / SNP)
rs3806642
rs3806642 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GFM1. Location: chromosome 3, position 158,362,038. Clinical significance in the table: Benign.
Reference-table entries
GFM1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:158362038
- Cytoband
- 3q25.32
- HGVS
- NM_024996.5(GFM1):c.-386G>T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.