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rs794726691

From SNPedia

ClinVar
Risk rs794726691(;)
Alt rs794726691(;)
Reference rs794726691(GCTG;GCTG)
Significance Pathogenic
Disease Mitochondrial complex III deficiency not provided
Variation info
Gene TTC19
CLNDBN Mitochondrial complex III deficiency, nuclear type 2 not provided
Reversed 0
HGVS NC_000017.10:g.15909807_15909810delGGCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000088675.3, RCV000201515.1,