Variant (rsID / SNP)
rs2290647
rs2290647 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRAMD1A. Location: chromosome 19, position 35,506,729. The table records no clinical significance for this variant.
Reference-table entries
GRAMD1ANot classified
- Variant type
- splice_acceptor_variant&intron_variant
- Chromosome / position
- 19:35506729
- HGVS
- NM_001320036.2,c.1331-2G>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.