List of variants in gene LPIN1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001349206.2(LPIN1):c.1729A>G (p.Ile577Val)	rs148499322	0.00173
NM_001349206.2(LPIN1):c.2661G>A (p.Pro887=)	rs114931326	0.00071
NM_001349206.2(LPIN1):c.1972G>A (p.Val658Ile)	rs146048019	0.00025
NM_001349206.2(LPIN1):c.1149C>T (p.Asp383=)	rs374756350
NM_001349206.2(LPIN1):c.1833T>C (p.Ala611=)
NM_001349206.2(LPIN1):c.2037C>T (p.Gly679=)
NM_001349206.2(LPIN1):c.501G>A (p.Leu167=)
NM_001349206.2(LPIN1):c.564G>C (p.Ser188=)	rs149765431

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