Variant (rsID / SNP)
rs570472222
rs570472222 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNE3. Location: chromosome 11, position 74,178,429. Clinical significance in the table: Benign.
Reference-table entries
KCNE3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:74178429
- Cytoband
- 11q13.4
- HGVS
- NM_005472.5(KCNE3):c.-190+14C>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.