Variant (rsID / SNP)
rs1803822
rs1803822 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IMPDH1. Location: chromosome 7, position 128,032,427. Clinical significance in the table: Benign.
Reference-table entries
IMPDH1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:128032427
- Cytoband
- 7q32.1
- HGVS
- NM_000883.4(IMPDH1):c.*634C>T
- Allele change
- Silent
Associated conditions / phenotypes
Retinitis pigmentosa|Leber congenital amaurosis 11
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.