Variant (rsID / SNP)
rs62351198
rs62351198 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ETFDH. Location: chromosome 4, position 159,603,110. Clinical significance in the table: Likely benign.
Reference-table entries
ETFDHLikely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:159603110
- Cytoband
- 4q32.1
- HGVS
- NM_004453.4(ETFDH):c.176-237A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.