Variant (rsID / SNP)
rs6766244
rs6766244 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZIC4. Location: chromosome 3, position 147,121,751. Clinical significance in the table: Benign.
Reference-table entries
ZIC4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:147121751
- Cytoband
- 3q24
- HGVS
- NM_032153.6(ZIC4):c.-15-1152G>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.