ClinVar Miner

List of variants in gene PEX6 reported as benign for not provided

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Gene type:
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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_000287.4(PEX6):c.1368-177G>A rs3805953 0.60522
NC_000006.12:g.42979275G>C rs9462860 0.57998
NM_000287.4(PEX6):c.1885-222A>G rs4714644 0.57658
NM_000287.4(PEX6):c.1046+162C>T rs9296407 0.57560
NM_000287.4(PEX6):c.2667-48G>A rs2274517 0.57547
NM_000287.4(PEX6):c.1688+30C>T rs9471982 0.56968
NM_000287.4(PEX6):c.1961+20G>A rs2274514 0.56870
NM_000287.4(PEX6):c.1885-24G>A rs3818554 0.56866
NM_000287.4(PEX6):c.2814G>A (p.Glu938=) rs1129186 0.56758
NM_000287.3(PEX6):c.-55C>T rs9462859 0.40581
NM_000287.4(PEX6):c.1367+230G>T rs3805951 0.40569
NM_000287.4(PEX6):c.399G>T (p.Val133=) rs9462858 0.40569
NM_000287.4(PEX6):c.2816C>A (p.Pro939Gln) rs1129187 0.40479
NM_000287.4(PEX6):c.883-3T>C rs9986447 0.36088
NM_000287.4(PEX6):c.883-230C>T rs2274518 0.11554
NM_000287.4(PEX6):c.1479+110C>T rs73432562 0.07370
NM_000287.4(PEX6):c.2426C>T (p.Ala809Val) rs35830695 0.07353
NM_000287.4(PEX6):c.2364G>A (p.Val788=) rs2274515 0.06152
NM_000287.4(PEX6):c.*319C>T rs736158 0.06143
NC_000006.12:g.42979453A>G rs41274896 0.06047
NM_000287.4(PEX6):c.1130+108T>C rs112436350 0.03524
NM_000287.4(PEX6):c.1130+106C>T rs57130470 0.02696
NM_000287.4(PEX6):c.1688+106del rs111981353 0.02605
NM_000287.4(PEX6):c.1884+110C>T rs112796168 0.02541
NM_000287.4(PEX6):c.207C>T (p.Pro69=) rs11539736 0.02141
NM_000287.4(PEX6):c.2644G>A (p.Val882Ile) rs2274516 0.02086
NM_000287.4(PEX6):c.1646C>T (p.Ala549Val) rs115960224 0.00687
NM_000287.4(PEX6):c.210G>A (p.Gly70=) rs398123304 0.00678
NM_000287.4(PEX6):c.1046+28T>C rs115079699 0.00667
NM_000287.4(PEX6):c.330C>G (p.Thr110=) rs140486558 0.00486
NM_000287.4(PEX6):c.1071A>G (p.Leu357=) rs116318004 0.00363
NM_000287.4(PEX6):c.1802G>A (p.Arg601Gln) rs34324426 0.00294
NM_000287.4(PEX6):c.1480-5C>T rs376473597 0.00126
NM_000287.4(PEX6):c.1234-8_1234-7dup rs200121485
NM_000287.4(PEX6):c.1367+280G>A rs3805952
NM_000287.4(PEX6):c.1480-123C>G rs113866814
NM_000287.4(PEX6):c.1885-111_1885-110del rs144477517
NM_000287.4(PEX6):c.235G>C (p.Ala79Pro) rs61752141
NM_000287.4(PEX6):c.882+129G>A rs111762254
NM_000287.4(PEX6):c.883-28del rs3831135

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