Variant (rsID / SNP)
rs149315279
rs149315279 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INVS. Location: chromosome 9, position 102,988,437. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
INVSConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:102988437
- Cytoband
- 9q31.1
- HGVS
- NM_014425.5(INVS):c.367C>T (p.Arg123Trp)
- Allele change
- Missense_R123W
Associated conditions / phenotypes
Nephronophthisis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.