Variants in gene LPL 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000237.3(LPL):c.106G>A (p.Asp36Asn)	rs1801177	0.01951
NM_000237.3(LPL):c.1018+16T>C	rs59184895	0.01380
NM_000237.3(LPL):c.953A>G (p.Asn318Ser)	rs268	0.01327
NM_000237.3(LPL):c.1279G>A (p.Ala427Thr)	rs5934	0.00972
NM_000237.3(LPL):c.430-6C>T	rs11570897	0.00432
NM_000237.3(LPL):c.1018+34A>G	rs190249506	0.00372
NM_000237.3(LPL):c.1135A>G (p.Thr379Ala)	rs300	0.00353
NM_000237.3(LPL):c.429+20A>C	rs3735959	0.00233
NM_000237.3(LPL):c.456T>C (p.Asn152=)	rs116678290	0.00183
NM_000237.3(LPL):c.1128C>T (p.Ile376=)	rs299	0.00140
NM_000237.3(LPL):c.1136C>T (p.Thr379Ile)	rs76708715	0.00133
NM_000237.3(LPL):c.-172_-171dup	rs146978295
NM_000237.3(LPL):c.213C>G (p.His71Gln)	rs11542065
NM_000237.3(LPL):c.276G>A (p.Val92=)	rs551959021
NM_000237.3(LPL):c.678A>G (p.Pro226=)	rs558390128

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