Variants in gene LPIN2 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 21

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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.-10+1313C>T	rs116643915	0.00793
NM_001375808.2(LPIN2):c.2327+11G>A	rs148930095	0.00240
NM_001375808.2(LPIN2):c.1735T>C (p.Ser579Pro)	rs150022314	0.00221
NM_001375808.2(LPIN2):c.1410C>T (p.Thr470=)	rs35932462	0.00159
NM_001375808.2(LPIN2):c.991G>T (p.Ala331Ser)	rs80338805	0.00142
NM_001375808.2(LPIN2):c.1159A>G (p.Lys387Glu)	rs104895501	0.00083
NM_001375808.2(LPIN2):c.1876C>T (p.Pro626Ser)	rs150806357	0.00083
NM_001375808.2(LPIN2):c.1815G>A (p.Ser605=)	rs143702044	0.00066
NM_001375808.2(LPIN2):c.1043C>T (p.Pro348Leu)	rs34676691	0.00051
NM_001375808.2(LPIN2):c.2568C>T (p.Leu856=)	rs149862905	0.00045
NM_001375808.2(LPIN2):c.2625G>A (p.Pro875=)	rs187572602	0.00025
NM_001375808.2(LPIN2):c.2445T>C (p.Asp815=)	rs140249737	0.00021
NM_001375808.2(LPIN2):c.2328-13A>T	rs199830303	0.00017
NM_001375808.2(LPIN2):c.608C>T (p.Ser203Phe)	rs144555528	0.00006
NM_001375808.2(LPIN2):c.1456+4C>G	rs373685201	0.00004
NM_001375808.2(LPIN2):c.2316C>T (p.Ser772=)	rs145270447	0.00003
NM_001375808.2(LPIN2):c.*90C>T	rs547359065
NM_001375808.2(LPIN2):c.1169-7del	rs746626720
NM_001375808.2(LPIN2):c.1169-7dup	rs746626720
NM_001375808.2(LPIN2):c.2621G>T (p.Cys874Phe)	rs201160155

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