Variant (rsID / SNP)
rs180177320
rs180177320 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRHPR. Location: chromosome 9, position 37,424,834. Clinical significance in the table: no interpretation for the single variant.
Reference-table entries
GRHPROther
- Clinical significance (as recorded)
- no interpretation for the single variant
- Variant type
- Deletion
- Chromosome / position
- 9:37424834
- Cytoband
- 9p13.2
- HGVS
- NM_012203.2(GRHPR):c.84-8_84-5del
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.