List of variants in gene LPL reported as benign for syndromic dyslipidemia

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_000237.3(LPL):c.*827A>T	rs3208305	0.36238
NM_000237.3(LPL):c.*1671T>C	rs13702	0.35875
NM_000237.3(LPL):c.*1846C>T	rs15285	0.35731
NM_000237.3(LPL):c.*1250A>G	rs3200218	0.19694
NM_000237.3(LPL):c.*796A>G	rs11570892	0.17851
NM_000237.3(LPL):c.1164C>A (p.Thr388=)	rs316	0.15994
NM_000237.3(LPL):c.*1142C>T	rs1059507	0.14544
NM_000237.3(LPL):c.*9G>A	rs4922115	0.14446
NM_000237.3(LPL):c.1018+82C>A	rs270	0.14245
NM_000237.3(LPL):c.*1742T>C	rs1059611	0.12946
NC_000008.11:g.19939160T>G	rs1800590	0.12919
NM_000237.3(LPL):c.*853C>T	rs1803924	0.09151
NM_000237.3(LPL):c.*1224C>A	rs3735964	0.09121
NM_000237.3(LPL):c.1421C>G (p.Ser474Ter)	rs328	0.08934
NM_000237.3(LPL):c.435G>A (p.Glu145=)	rs248	0.05843
NM_000237.3(LPL):c.405G>A (p.Val135=)	rs1121923	0.04960
NM_000237.3(LPL):c.*371T>C	rs3289	0.04016
NM_000237.3(LPL):c.*1416T>C	rs58998793	0.02343
NM_000237.3(LPL):c.*1783A>T	rs17091815	0.02107
NM_000237.3(LPL):c.106G>A (p.Asp36Asn)	rs1801177	0.01951
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.-283G>T	rs80351041	0.00790
NM_000237.3(LPL):c.*1291G>A	rs139240067	0.00549
NM_000237.3(LPL):c.*1928T>C	rs79756214	0.00516
NM_000237.3(LPL):c.*29G>A	rs7818177	0.00511
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.*949G>A	rs11570893	0.00168
NM_000237.3(LPL):c.345A>C (p.Ser115=)	rs147309575	0.00088
NM_000237.3(LPL):c.798C>T (p.Cys266=)	rs118204082	0.00034
NM_000237.3(LPL):c.*1848C>A	rs3866471
NM_000237.3(LPL):c.290C>T (p.Ala97Val)	rs201946950
NM_000237.3(LPL):c.678A>G (p.Pro226=)	rs558390128

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