Variant (rsID / SNP)

rs10069690

rs10069690 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TERT. Location: chromosome 5, position 1,279,790. Clinical significance in the table: Benign.

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Reference-table entries

TERTBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:1279790
Cytoband: 5p15.33
HGVS: NM_198253.3(TERT):c.1951-205G>A
Allele change: Silent

Associated conditions / phenotypes

Chronic osteomyelitis|Idiopathic Pulmonary Fibrosis|Dyskeratosis congenita, autosomal dominant 2

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.