ClinVar Miner

List of variants reported as risk factor for hypertriglyceridemia

Included ClinVar conditions (6):

Coronary artery disorder; Hypertriglyceridemia; Hypertensive disorder; Diabetes
Familial type 5 hyperlipoproteinemia; Hypertriglyceridemia 1
Hypertelorism; Hyperhydroxyprolinemia; Enuresis; Sleep abnormality; Tall stature; Eczematoid dermatitis; Delayed speech and language development; Frontal bossing; Triangular face; Thin upper lip vermilion; Recurrent otitis media; Microdontia; Neutropenia; Hypertriglyceridemia; Downturned corners of mouth; Increased blood urea nitrogen; Hypertyrosinemia; Somatic sensory dysfunction; Delayed fine motor development; Abnormal circulating serine family amino acid concentration; Bronchiolitis; Monocytopenia; Abnormal emotional state; Encopresis; Asthma
Hypertriglyceridemia
Hypertriglyceridemia 1
Hypertriglyceridemia 2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001371904.1(APOA5):c.*158C>T	rs2266788	0.93650
NM_001371904.1(APOA5):c.553G>T (p.Gly185Cys)	rs2075291	0.00514
NM_001371904.1(APOA5):c.56C>G (p.Ser19Trp)	rs3135506
NM_032607.3(CREB3L3):c.138G>A (p.Trp46Ter)
NM_032607.3(CREB3L3):c.[732dup;739A>T]

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