Variant (rsID / SNP)
rs76975466
rs76975466 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INVS. Location: chromosome 9, position 102,888,877. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
INVSBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:102888877
- Cytoband
- 9q31.1
- HGVS
- NM_014425.5(INVS):c.273+46C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.