List of variants in gene SRPX2 reported as likely benign by GeneDx

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_014467.3(SRPX2):c.82+243C>T	rs56259360	0.02038
NM_014467.3(SRPX2):c.164-158T>G	rs112895781	0.01550
NM_014467.3(SRPX2):c.1095+237G>A	rs58820687	0.01309
NM_014467.3(SRPX2):c.*60G>A	rs148234042	0.01006
NM_014467.3(SRPX2):c.164-234T>G	rs1355559214	0.00764
NM_014467.3(SRPX2):c.782-189C>T	rs150597837	0.00528
NM_014467.3(SRPX2):c.163+293G>T	rs192186175	0.00520
NM_014467.3(SRPX2):c.782-27C>T	rs149678452	0.00507
NM_014467.3(SRPX2):c.533-117T>C	rs181200947	0.00447
NM_014467.3(SRPX2):c.1095+276G>A	rs6652817	0.00435
NM_014467.3(SRPX2):c.533-30G>A	rs185564106	0.00374
NM_014467.3(SRPX2):c.164-231T>G	rs867705358	0.00368
NM_014467.3(SRPX2):c.840G>A (p.Ala280=)	rs139377205	0.00118
NM_014467.3(SRPX2):c.323G>A (p.Ser108Asn)	rs200483534	0.00023
NM_014467.3(SRPX2):c.693C>A (p.His231Gln)	rs142719253	0.00022
NM_014467.3(SRPX2):c.449C>T (p.Ser150Phe)	rs373847965	0.00019
NM_014467.3(SRPX2):c.564C>T (p.His188=)	rs149317696	0.00015
NM_014467.3(SRPX2):c.1199A>G (p.Asn400Ser)	rs141292909	0.00011
NM_014467.3(SRPX2):c.893G>A (p.Arg298His)	rs369663551	0.00011
NM_014467.3(SRPX2):c.257G>A (p.Arg86His)	rs776691028	0.00010
NM_014467.3(SRPX2):c.962-16C>T	rs190642591	0.00006
NM_014467.3(SRPX2):c.-37A>G	rs796053341	0.00002
NM_014467.3(SRPX2):c.1064G>A (p.Arg355Gln)	rs541303724	0.00002
NM_014467.3(SRPX2):c.1229G>A (p.Arg410His)	rs368571175	0.00002
NM_014467.3(SRPX2):c.1165G>A (p.Val389Met)	rs1453303256	0.00001
NM_014467.3(SRPX2):c.1202T>C (p.Ile401Thr)	rs796053346	0.00001
NM_014467.3(SRPX2):c.1217+35G>C	rs201768337
NM_014467.3(SRPX2):c.164-218_164-217del	rs771852530
NM_014467.3(SRPX2):c.605G>A (p.Arg202Gln)	rs200784551
NM_014467.3(SRPX2):c.928C>T (p.Arg310Cys)	rs758448998

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