ClinVar Miner

List of variants in gene SRPX2 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_014467.3(SRPX2):c.781+321G>A rs1419017 0.89523
NM_014467.3(SRPX2):c.356-38G>A rs2022475 0.83087
NM_014467.3(SRPX2):c.356-295T>C rs5921620 0.29374
NM_014467.3(SRPX2):c.-399G>C rs1343213 0.13943
NM_014467.3(SRPX2):c.356-205C>A rs36224186 0.09028
NM_014467.3(SRPX2):c.1096-119T>C rs113945055 0.05949
NM_014467.3(SRPX2):c.355+152C>A rs55796803 0.05805
NM_014467.3(SRPX2):c.83-100T>C rs2073164 0.04791
NM_014467.3(SRPX2):c.163+291T>G rs2073165 0.04723
NM_014467.3(SRPX2):c.163+12T>C rs73555462 0.02331
NM_014467.3(SRPX2):c.164-25G>T rs41293523 0.01923
NM_014467.3(SRPX2):c.1217+36G>C rs182041986 0.00576
NM_014467.3(SRPX2):c.460C>G (p.His154Asp) rs73636611 0.00298
NM_014467.3(SRPX2):c.1373G>A (p.Arg458Gln) rs146051561 0.00133
NM_014467.3(SRPX2):c.660-16del rs764480482 0.00115
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.961+12C>T rs373436594 0.00031
NM_014467.3(SRPX2):c.809C>T (p.Pro270Leu) rs148735447 0.00030
NM_014467.3(SRPX2):c.1218-6C>T rs370981134 0.00019
NM_014467.3(SRPX2):c.624G>A (p.Pro208=) rs139514583 0.00018
NM_014467.3(SRPX2):c.164-217del rs771852530
NM_014467.3(SRPX2):c.164-217dup rs771852530

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