List of variants in gene ADAMTS2 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_014244.5(ADAMTS2):c.2480G>A (p.Arg827Gln)	rs35445112	0.02575
NM_014244.5(ADAMTS2):c.*2196T>A	rs147985762	0.01159
NM_014244.5(ADAMTS2):c.68T>C (p.Leu23Pro)	rs565885690	0.00707
NM_014244.5(ADAMTS2):c.*816C>T	rs116130524	0.00690
NM_014244.5(ADAMTS2):c.*977G>A	rs138084603	0.00451
NM_014244.5(ADAMTS2):c.1458C>T (p.Tyr486=)	rs61757478	0.00427
NM_014244.5(ADAMTS2):c.*2587T>C	rs140304884	0.00414
NM_014244.5(ADAMTS2):c.2751-4G>A	rs112155474	0.00324
NM_014244.5(ADAMTS2):c.1488C>T (p.Phe496=)	rs147438064	0.00184
NM_014244.5(ADAMTS2):c.*2141G>T	rs77882118	0.00149
NM_014244.5(ADAMTS2):c.*1573A>C	rs560216364	0.00080
NM_014244.5(ADAMTS2):c.764G>A (p.Arg255Gln)	rs117222015	0.00048
NM_014244.5(ADAMTS2):c.*2397G>A	rs117141618	0.00036
NM_014244.5(ADAMTS2):c.*1797C>T	rs553329835	0.00026
NM_014244.5(ADAMTS2):c.*2420A>G	rs376369089	0.00012
NM_014244.5(ADAMTS2):c.1437_1438del	rs375426260
NM_014244.5(ADAMTS2):c.1579_1585del	rs539443462
NM_014244.5(ADAMTS2):c.1308G>A (p.Ala436=)	rs41285549
NM_014244.5(ADAMTS2):c.47TGC[7] (p.Leu23del)	rs568040559

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