Variant (rsID / SNP)
rs383362
rs383362 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WWOX, MAF. Location: chromosome 16, position 79,245,820. The table records no clinical significance for this variant.
Reference-table entries
WWOXNot classified
- Variant type
- 3_prime_UTR_variant
- Chromosome / position
- 16:79245820
- HGVS
- NM_016373.4,c.*127G>T
- Allele change
- Silent
Associated conditions / phenotypes
Osteogenic Sarcoma|Lung Cancer Susceptibility 3|Cervical Cancer|Adenocarcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.