Variant (rsID / SNP)
rs4685074
rs4685074 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM43. Location: chromosome 3, position 14,173,963. Clinical significance in the table: Benign.
Reference-table entries
TMEM43Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:14173963
- Cytoband
- 3p25.1
- HGVS
- NM_024334.3(TMEM43):c.393-83G>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.