List of variants in gene SRPX2 reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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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.893G>A (p.Arg298His)	rs369663551	0.00011
NM_014467.3(SRPX2):c.248T>C (p.Leu83Pro)	rs141168255	0.00007
NM_014467.3(SRPX2):c.542C>G (p.Pro181Arg)	rs769478434	0.00004
NM_014467.3(SRPX2):c.671G>A (p.Arg224Gln)	rs763624310	0.00003
NM_014467.3(SRPX2):c.961+1G>A	rs1303998333	0.00002
NM_014467.3(SRPX2):c.1255G>A (p.Val419Met)	rs797046012	0.00001
NM_014467.3(SRPX2):c.164T>C (p.Val55Ala)	rs777972842	0.00001
NM_014467.3(SRPX2):c.1393G>A (p.Glu465Lys)	rs898722174
NM_014467.3(SRPX2):c.355+1G>C
NM_014467.3(SRPX2):c.515G>A (p.Gly172Asp)	rs775513104

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