Variant (rsID / SNP)
rs150663325
rs150663325 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF125. Location: chromosome 18, position 29,645,930. Clinical significance in the table: Benign.
Reference-table entries
RNF125Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 18:29645930
- Cytoband
- 18q12.1
- HGVS
- NM_017831.4(RNF125):c.570A>T (p.Arg190Ser)
- Allele change
- Missense_R190S
Associated conditions / phenotypes
Tenorio syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.