List of variants in gene LPIN2 reported as likely benign for not specified

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001375808.2(LPIN2):c.1801G>A (p.Glu601Lys)	rs61735393	0.00824
NM_001375808.2(LPIN2):c.2327+11G>A	rs148930095	0.00240
NM_001375808.2(LPIN2):c.1815G>A (p.Ser605=)	rs143702044	0.00066
NM_001375808.2(LPIN2):c.516C>T (p.Ala172=)	rs150312425	0.00026
NM_001375808.2(LPIN2):c.2088-7T>G	rs199713353	0.00011
NM_001375808.2(LPIN2):c.2371C>T (p.Leu791=)	rs373520277	0.00011
NM_001375808.2(LPIN2):c.2327+14A>G	rs370048111	0.00010
NM_001375808.2(LPIN2):c.289-16C>T	rs759180126	0.00010
NM_001375808.2(LPIN2):c.1281C>T (p.Pro427=)	rs778559792	0.00004
NM_001375808.2(LPIN2):c.540A>C (p.Thr180=)	rs151135579	0.00003
NM_001375808.2(LPIN2):c.1347C>T (p.Ser449=)	rs773074044	0.00002
NM_001375808.2(LPIN2):c.1299C>T (p.Pro433=)	rs781673368	0.00001
NM_001375808.2(LPIN2):c.2443-14A>G	rs749926941	0.00001
NM_001375808.2(LPIN2):c.2484A>G (p.Arg828=)	rs761194035	0.00001
NM_001375808.2(LPIN2):c.-4A>G	rs1555678614
NM_001375808.2(LPIN2):c.1621-18C>G	rs375819924
NM_001375808.2(LPIN2):c.1812C>A (p.Ser604=)	rs879254186
NM_001375808.2(LPIN2):c.193-9C>T	rs1555677691
NM_001375808.2(LPIN2):c.1939-5A>G	rs779830291
NM_001375808.2(LPIN2):c.2327+9C>A	rs536913334
NM_001375808.2(LPIN2):c.2327+9C>T	rs536913334
NM_001375808.2(LPIN2):c.2328-15_2328-10del	rs770202563
NM_001375808.2(LPIN2):c.2400G>A (p.Pro800=)	rs747097533
NM_001375808.2(LPIN2):c.2427T>C (p.Phe809=)	rs1057520415

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