Variant (rsID / SNP)
rs35267264
rs35267264 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WASHC4. Location: chromosome 12, position 105,519,873. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
WASHC4Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:105519873
- Cytoband
- 12q23.3
- HGVS
- NM_015275.3(WASHC4):c.878G>A (p.Arg293Gln)
- Allele change
- Missense_R293Q
Associated conditions / phenotypes
Inborn genetic diseases
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.