ClinVar Miner

List of variants in gene PEX1 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_000466.3(PEX1):c.2331C>A (p.Gly777=) rs10278857 0.93013
NM_000466.3(PEX1):c.1804-144A>T rs6465359 0.91679
NM_000466.3(PEX1):c.1359+155C>A rs38807 0.87539
NM_000466.3(PEX1):c.358-15G>A rs38809 0.86650
NM_000466.3(PEX1):c.2584-245A>T rs10953071 0.86496
NM_000466.3(PEX1):c.1670+219T>C rs11767684 0.31565
NM_000466.3(PEX1):c.1484-36G>A rs2111200 0.25489
NM_000466.3(PEX1):c.1671-314C>T rs7791858 0.24006
NM_000466.3(PEX1):c.2718+183C>A rs10269874 0.12962
NM_000466.3(PEX1):c.1804-28G>A rs10236856 0.07802
NM_000466.3(PEX1):c.1803+235A>G rs7809455 0.05706
NM_000466.3(PEX1):c.2417-42T>C rs3213609 0.05567
NM_000466.3(PEX1):c.2719-244G>A rs73710409 0.05413
NM_000466.3(PEX1):c.358-11G>C rs113104510 0.04153
NM_000466.3(PEX1):c.1240-279G>A rs112904813 0.04145
NM_000466.3(PEX1):c.473-18G>A rs2066743 0.03344
NM_000466.3(PEX1):c.1360-336A>C rs61492841 0.02935
NM_000466.3(PEX1):c.2088A>G (p.Ile696Met) rs35996821 0.02553
NM_000466.3(PEX1):c.2226+139A>G rs111474000 0.01659
NM_000466.3(PEX1):c.1671-7T>C rs74519968 0.01312
NM_000466.3(PEX1):c.130-180del rs71841826
NM_000466.3(PEX1):c.1484-95del rs5885807
NM_000466.3(PEX1):c.1484-96_1484-95del rs5885807
NM_000466.3(PEX1):c.1670+193del rs202132988
NM_000466.3(PEX1):c.1671-120del rs79143453
NM_000466.3(PEX1):c.1671-66dup rs79002315
NM_000466.3(PEX1):c.1900+142_1900+143insTCTTAGAAATTTTAAG rs11269897
NM_000466.3(PEX1):c.2583+136del rs3842627
NM_000466.3(PEX1):c.2584-10del rs5885806
NM_000466.3(PEX1):c.2584-11_2584-10del rs5885806
NM_000466.3(PEX1):c.2584-21dup rs5885806

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