List of variants in gene combination HSPG2, LDLRAD2 reported as likely benign by Athena Diagnostics Inc

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005529.7(HSPG2):c.12874G>A (p.Glu4292Lys)	rs141280063	0.00135
NM_005529.7(HSPG2):c.12842G>A (p.Arg4281His)	rs151184052	0.00118
NM_005529.7(HSPG2):c.13033G>A (p.Gly4345Arg)	rs148788926	0.00045
NM_005529.7(HSPG2):c.13026G>A (p.Thr4342=)	rs151237224	0.00005
NM_005529.7(HSPG2):c.13011C>T (p.Ala4337=)	rs1263243391
NM_005529.7(HSPG2):c.13089G>A (p.Ser4363=)	rs573792702

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