Variant (rsID / SNP)
rs6552113
rs6552113 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GNRHR. Location: chromosome 4, position 68,620,957. Clinical significance in the table: Benign.
Reference-table entries
GNRHRBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:68620957
- Cytoband
- 4q13.2
- HGVS
- NM_000406.2(GNRHR):c.-904A>G
- Allele change
- Silent
Associated conditions / phenotypes
Hypogonadotropic hypogonadism 7 with or without anosmia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.