List of variants in gene SRPX2 reported as benign for childhood-onset epilepsy syndrome

Minimum submission review status:		Collection method:
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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_014467.3(SRPX2):c.356-38G>A	rs2022475	0.83087
NM_014467.3(SRPX2):c.163+12T>C	rs73555462	0.02331
NM_014467.3(SRPX2):c.460C>G (p.His154Asp)	rs73636611	0.00298
NM_014467.3(SRPX2):c.840G>A (p.Ala280=)	rs139377205	0.00118
NM_014467.3(SRPX2):c.481C>A (p.Arg161=)	rs150552508	0.00101
NM_014467.3(SRPX2):c.918T>C (p.Cys306=)	rs34728871	0.00080
NM_014467.3(SRPX2):c.1293C>T (p.Tyr431=)	rs138091242	0.00050
NM_014467.3(SRPX2):c.980A>G (p.Asn327Ser)	rs121918363	0.00041
NM_014467.3(SRPX2):c.323G>A (p.Ser108Asn)	rs200483534	0.00023
NM_014467.3(SRPX2):c.1218-6C>T	rs370981134	0.00019

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