List of variants in gene LPIN1 reported as pathogenic by GeneDx

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001349206.2(LPIN1):c.1807-2A>G	rs533651991	0.00007
NM_001349206.2(LPIN1):c.1270C>T (p.Arg424Ter)	rs119480072	0.00006
NM_001349206.2(LPIN1):c.181C>T (p.Arg61Ter)	rs747835893	0.00001
NM_001349206.2(LPIN1):c.2509C>T (p.Arg837Ter)	rs119480073

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