Variant (rsID / SNP)

rs117087989

rs117087989 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTC19. Location: chromosome 17, position 15,931,171. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TTC19Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 17:15931171
Cytoband: 17p12
HGVS: NM_017775.4(TTC19):c.*335C>T
Allele change: Silent

Associated conditions / phenotypes

Mitochondrial complex III deficiency nuclear type 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.