Variant (rsID / SNP)
rs7637449
rs7637449 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC66. Location: chromosome 3, position 56,628,031. The table records no clinical significance for this variant.
Reference-table entries
CCDC66Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:56628031
- HGVS
- NM_001353147.1,c.1379G>A,p.Arg460Gln
- Allele change
- Silent
Associated conditions / phenotypes
Missense_R426Q|Silent|Missense_R410Q|Missense_R426Q|Silent|Silent|Missense_R460Q|Missense_R437Q|Missense_R96Q|Silent|Missense_R118Q|Silent|Missense_R460Q|Silent|Missense_R161Q|Missense_R426Q|Silent|Missense_R417Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.