Variant (rsID / SNP)
rs6979
rs6979 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACD. Location: chromosome 16, position 67,691,668. The table records no clinical significance for this variant.
Reference-table entries
ACDNot classified
- Variant type
- missense_variant
- Chromosome / position
- 16:67691668
- HGVS
- NM_001082486.2,c.1295T>C,p.Val432Ala
- Allele change
- Missense_V429A
Associated conditions / phenotypes
Inflammatory Spondylopathy|Spondyloarthropathy 1|Spondylitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.