Variant (rsID / SNP)
rs11049488
rs11049488 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC91. Location: chromosome 12, position 28,412,372. The table records no clinical significance for this variant.
Reference-table entries
CCDC91Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:28412372
- HGVS
- NM_001352078.2,c.106G>A,p.Ala36Thr
- Allele change
- Missense_A36T
Associated conditions / phenotypes
Missense_A36T|Silent|Missense_A36T|Silent|Missense_A36T|Missense_A36T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.