Variants in gene SRPX2 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_014467.3(SRPX2):c.460C>G (p.His154Asp)	rs73636611	0.00298
NM_014467.3(SRPX2):c.1030C>A (p.Leu344Ile)	rs149051060	0.00145
NM_014467.3(SRPX2):c.840G>A (p.Ala280=)	rs139377205	0.00118
NM_014467.3(SRPX2):c.980A>G (p.Asn327Ser)	rs121918363	0.00041
NM_014467.3(SRPX2):c.693C>A (p.His231Gln)	rs142719253	0.00022
NM_014467.3(SRPX2):c.893G>A (p.Arg298His)	rs369663551	0.00011
NM_014467.3(SRPX2):c.248T>C (p.Leu83Pro)	rs141168255	0.00007
NM_014467.3(SRPX2):c.224A>T (p.Lys75Met)	rs767072861	0.00005
NM_014467.3(SRPX2):c.605G>A (p.Arg202Gln)	rs200784551

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