Variant (rsID / SNP)
rs41276676
rs41276676 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGD4. Location: chromosome 12, position 32,754,367. Clinical significance in the table: Benign.
Reference-table entries
FGD4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:32754367
- Cytoband
- 12p11.21
- HGVS
- NM_001370298.3(FGD4):c.1247+10G>T
- Allele change
- Silent
Associated conditions / phenotypes
Charcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4H|Charcot-Marie-Tooth disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.