Variant (rsID / SNP)
rs56401536
rs56401536 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRHPR. Location: chromosome 9, position 37,430,652. Clinical significance in the table: Benign.
Reference-table entries
GRHPRBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:37430652
- Cytoband
- 9p13.2
- HGVS
- NM_012203.2(GRHPR):c.734+9G>A
- Allele change
- Silent
Associated conditions / phenotypes
Primary hyperoxaluria, type II
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.