Variant (rsID / SNP)

rs199473679

rs199473679 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CTC1. Location: chromosome 17, position 8,133,264. Clinical significance in the table: Pathogenic.

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Reference-table entries

CTC1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Microsatellite
Chromosome / position: 17:8133264
Cytoband: 17p13.1
HGVS: NM_025099.6(CTC1):c.2951GTT[1] (p.Cys985del)

Associated conditions / phenotypes

Cerebroretinal microangiopathy with calcifications and cysts 1|Dyskeratosis congenita|Coats plus syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.