Variant (rsID / SNP)
rs9102
rs9102 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GSN. Location: chromosome 9, position 124,094,800. Clinical significance in the table: Benign.
Reference-table entries
GSNBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:124094800
- Cytoband
- 9q33.2
- HGVS
- NM_198252.3(GSN):c.2115T>C (p.Phe705=)
- Allele change
- Synonymous_F705F
Associated conditions / phenotypes
Meretoja syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.