List of variants in gene LTBP2 reported as likely benign by Illumina Laboratory Services, Illumina

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_000428.3(LTBP2):c.*1873C>G	rs77847288	0.04063
NM_000428.3(LTBP2):c.2715C>T (p.Arg905=)	rs7145480	0.02571
NM_000428.3(LTBP2):c.3093C>T (p.Ser1031=)	rs45473602	0.02563
NM_000428.3(LTBP2):c.*2153T>C	rs113879332	0.02134
NM_000428.3(LTBP2):c.4263G>A (p.Ala1421=)	rs61738017	0.01972
NM_000428.3(LTBP2):c.1021+14G>A	rs150408645	0.01681
NM_000428.3(LTBP2):c.3852C>T (p.Arg1284=)	rs61736977	0.01652
NM_000428.3(LTBP2):c.*2463G>T	rs10141546	0.01598
NM_000428.3(LTBP2):c.*2044G>A	rs73296214	0.01534
NM_000428.3(LTBP2):c.915G>A (p.Thr305=)	rs60337900	0.01390
NM_000428.3(LTBP2):c.*2684A>G	rs74384554	0.01012
NM_000428.3(LTBP2):c.1553G>T (p.Ser518Ile)	rs137854857	0.00812
NM_000428.3(LTBP2):c.4089C>T (p.Asn1363=)	rs141318496	0.00600
NM_000428.3(LTBP2):c.378C>T (p.Pro126=)	rs140842900	0.00528
NM_000428.3(LTBP2):c.*119C>T	rs146119949	0.00526
NM_000428.3(LTBP2):c.3891G>A (p.Pro1297=)	rs61738013	0.00500
NM_000428.3(LTBP2):c.1399+10G>T	rs143528294	0.00488
NM_000428.3(LTBP2):c.3527-3C>A	rs138194436	0.00364
NM_000428.3(LTBP2):c.4203G>A (p.Thr1401=)	rs150977380	0.00305
NM_000428.3(LTBP2):c.450G>T (p.Arg150=)	rs111342797	0.00290
NM_000428.3(LTBP2):c.*2363A>G	rs190461277	0.00211
NM_000428.3(LTBP2):c.4467T>C (p.Cys1489=)	rs80088294	0.00165
NM_000428.3(LTBP2):c.4286G>A (p.Arg1429Gln)	rs116914994	0.00133
NM_000428.3(LTBP2):c.4621G>A (p.Glu1541Lys)	rs143456909	0.00121
NM_000428.3(LTBP2):c.4911C>T (p.Asn1637=)	rs12586758	0.00074
NM_000428.3(LTBP2):c.*945T>C	rs374130664	0.00042
NM_000428.3(LTBP2):c.*1427A>G	rs187052141	0.00024
NM_000428.3(LTBP2):c.2160C>T (p.Phe720=)	rs74758312	0.00023
NM_000428.3(LTBP2):c.110G>T (p.Arg37Met)	rs934996

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