Variant (rsID / SNP)
rs1133028
rs1133028 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC91. Location: chromosome 12, position 28,603,112. The table records no clinical significance for this variant.
Reference-table entries
CCDC91Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:28603112
- HGVS
- NM_001352078.2,c.781A>G,p.Met261Val
- Allele change
- Missense_M225V
Associated conditions / phenotypes
Missense_M261V|Missense_M231V|Missense_M261V|Missense_M99V|Missense_M261V|Missense_M261V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.