ClinVar Miner

List of variants in gene PRSS56 reported as benign by GeneDx

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_001195129.2(PRSS56):c.706+64A>G rs733603 0.83544
NM_001195129.2(PRSS56):c.1251T>G (p.Pro417=) rs2741299 0.83022
NM_001195129.2(PRSS56):c.205+91T>C rs2853444 0.82398
NC_000002.12:g.232520315G>A rs2573210 0.74498
NM_001195129.2(PRSS56):c.1522-8A>G rs2853447 0.70005
NM_001195129.2(PRSS56):c.88G>A (p.Ala30Thr) rs1550094 0.64904
NM_001195129.2(PRSS56):c.1415-122C>T rs2853446 0.45513
NM_001195129.2(PRSS56):c.256+7T>C rs2853445 0.45350
NM_001195129.2(PRSS56):c.-107C>T rs2741294 0.28457
NM_001195129.2(PRSS56):c.1414+88G>C rs58091792 0.24172
NM_001195129.2(PRSS56):c.1012+23C>T rs733602 0.23899
NM_001195129.2(PRSS56):c.98-63C>T rs62193795 0.08775
NM_001195129.2(PRSS56):c.97+27C>T rs116445642 0.06567
NM_001195129.2(PRSS56):c.1186+31G>A rs79792358 0.05915
NM_001195129.2(PRSS56):c.547-33T>C rs115599535 0.04501
NM_001195129.2(PRSS56):c.1795C>G (p.Pro599Ala) rs61744404 0.04318
NM_001195129.2(PRSS56):c.98-143C>T rs79872260 0.02168
NM_001195129.2(PRSS56):c.205+14C>A rs552107195 0.01064
NM_001195129.2(PRSS56):c.1419C>T (p.Cys473=) rs145395409 0.00550
NM_001195129.2(PRSS56):c.205+10C>G rs77311538 0.00227
NM_001195129.2(PRSS56):c.205+18del rs370334682
NM_001195129.2(PRSS56):c.205+190C>T rs2741295
NM_001195129.2(PRSS56):c.206-94G>A rs11902035
NM_001195129.2(PRSS56):c.98-42C>G rs115367581

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