Variant (rsID / SNP)

rs79724115

rs79724115 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTC19. Location: chromosome 17, position 15,903,056. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TTC19Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 17:15903056
Cytoband: 17p12
HGVS: NM_017775.3(TTC19):c.-107A>T
Allele change: Silent

Associated conditions / phenotypes

Mitochondrial complex III deficiency nuclear type 1

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.