Variant (rsID / SNP)
rs7383287
rs7383287 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HLA-DOB. Location: chromosome 6, position 32,783,086. The table records no clinical significance for this variant.
Reference-table entries
HLA-DOBNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:32783086
- HGVS
- NM_002120.4,c.96T>C,p.Asp32Asp
- Allele change
- Synonymous_D32D
Associated conditions / phenotypes
Hepatitis C|Hepatitis C Virus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.