Variants in gene LPIN2 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001375808.2(LPIN2):c.991G>T (p.Ala331Ser)	rs80338805	0.00142
NM_001375808.2(LPIN2):c.2625G>A (p.Pro875=)	rs187572602	0.00025
NM_001375808.2(LPIN2):c.2328-13A>T	rs199830303	0.00017
NM_001375808.2(LPIN2):c.1169-7del	rs746626720
NM_001375808.2(LPIN2):c.2621G>T (p.Cys874Phe)	rs201160155

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