Variant (rsID / SNP)
rs3735819
rs3735819 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GATA4. Location: chromosome 8, position 11,606,312. Clinical significance in the table: Benign.
Reference-table entries
GATA4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 8:11606312
- Cytoband
- 8p23.1
- HGVS
- NM_001308093.3(GATA4):c.617-113T>C
- Allele change
- Silent
Associated conditions / phenotypes
Congenital heart disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.