Variant (rsID / SNP)
rs6899628
rs6899628 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLH. Location: chromosome 6, position 43,582,584. Clinical significance in the table: Benign.
Reference-table entries
POLHBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 6:43582584
- Cytoband
- 6p21.1
- HGVS
- NM_006502.3(POLH):c.*290C>T
- Allele change
- Synonymous_D787D
Associated conditions / phenotypes
Xeroderma pigmentosum variant type
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.