List of variants in gene LPL reported as likely pathogenic by Ambry Genetics

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

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000237.3(LPL):c.292G>A (p.Ala98Thr)	rs145657341	0.00006
NM_000237.3(LPL):c.589C>T (p.Arg197Cys)	rs768128481	0.00004
NM_000237.3(LPL):c.662T>C (p.Ile221Thr)	rs118204061	0.00004
NM_000237.3(LPL):c.1139+1G>A	rs767260655	0.00001
NM_000237.3(LPL):c.1187A>T (p.Glu396Val)	rs886037775
NM_000237.3(LPL):c.242G>A (p.Gly81Asp)	rs762007406

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