Variant (rsID / SNP)
rs33983156
rs33983156 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC12. Location: chromosome 3, position 46,965,111. The table records no clinical significance for this variant.
Reference-table entries
CCDC12Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:46965111
- HGVS
- NM_144716.6,c.331G>A,p.Val111Ile
- Allele change
- Missense_V111I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.