Variant (rsID / SNP)
rs547154
rs547154 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C2. Location: chromosome 6, position 31,910,938. Clinical significance in the table: protective.
Reference-table entries
C2Protective
- Clinical significance (as recorded)
- protective
- Variant type
- single nucleotide variant
- Chromosome / position
- 6:31910938
- Cytoband
- 6p21.33
- HGVS
- NM_000063.6(C2):c.1360+62G>T
- Allele change
- Silent
Associated conditions / phenotypes
Age related macular degeneration 14
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.