Variant (rsID / SNP)
rs3841128
rs3841128 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRIA1. Location: chromosome 5, position 152,871,788. Clinical significance in the table: Benign.
Reference-table entries
GRIA1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- Duplication
- Chromosome / position
- 5:152871788
- Cytoband
- 5q33.2
- HGVS
- NM_000827.4(GRIA1):c.82+1259dup
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.