Variant (rsID / SNP)
rs1143684
rs1143684 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NQO2. Location: chromosome 6, position 3,010,390. The table records no clinical significance for this variant.
Reference-table entries
NQO2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:3010390
- HGVS
- NM_000904.6,c.139C>T,p.Leu47Phe
- Allele change
- Missense_L47F
Associated conditions / phenotypes
Mucositis|Leukemia|Thrombocytopenia|Leukemia, Acute Myeloid|Myeloid Leukemia|Pancreatic Cancer|Toxic Encephalopathy|Neuroblastoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.