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

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_000466.3(PEX1):c.1360-209G>A	rs6946364	0.03237
NM_000466.3(PEX1):c.2718+134A>G	rs76587269	0.02817
NM_000466.3(PEX1):c.2584-20T>A	rs111535201	0.02687
NM_000466.3(PEX1):c.2088A>G (p.Ile696Met)	rs35996821	0.02553
NM_000466.3(PEX1):c.1671-7T>C	rs74519968	0.01312
NM_000466.3(PEX1):c.1239+161C>G	rs113848550	0.00886
NM_000466.3(PEX1):c.812A>G (p.Asn271Ser)	rs138183109	0.00874
NM_000466.3(PEX1):c.1521G>C (p.Trp507Cys)	rs112822975	0.00803
NM_000466.3(PEX1):c.1484-106A>G	rs200489532	0.00720
NM_000466.3(PEX1):c.2271G>C (p.Leu757Phe)	rs142838522	0.00270
NM_000466.3(PEX1):c.934A>G (p.Ile312Val)	rs146312634	0.00223
NM_000466.3(PEX1):c.330C>G (p.Pro110=)	rs71560821	0.00218
NM_000466.3(PEX1):c.1579A>G (p.Thr527Ala)	rs144942544	0.00217
NM_000466.3(PEX1):c.2442C>T (p.Phe814=)	rs145430946	0.00216
NM_000466.3(PEX1):c.473-3C>T	rs150576000	0.00213
NM_000466.3(PEX1):c.637C>T (p.Leu213Phe)	rs141798874	0.00185
NM_000466.3(PEX1):c.2640T>C (p.Tyr880=)	rs201719745	0.00022
NM_000466.3(PEX1):c.2584-9G>T	rs370692491	0.00020
NM_000466.3(PEX1):c.159C>T (p.His53=)	rs200950057	0.00014
NM_000466.3(PEX1):c.1284C>T (p.Ala428=)	rs145153467	0.00006
NM_000466.3(PEX1):c.147G>A (p.Val49=)	rs202230667	0.00005
NM_000466.3(PEX1):c.2124G>C (p.Leu708=)	rs200258130	0.00004
NM_000466.3(PEX1):c.282C>G (p.Leu94=)	rs201368809	0.00001
NM_000466.3(PEX1):c.1142C>A (p.Ala381Asp)	rs73404416
NM_000466.3(PEX1):c.1230G>A (p.Gly410=)	rs539382251
NM_000466.3(PEX1):c.1803+185_1803+187del	rs150645900
NM_000466.3(PEX1):c.2205A>G (p.Gln735=)	rs201308230
NM_000466.3(PEX1):c.2226+57del	rs138118520
NM_000466.3(PEX1):c.468A>G (p.Gln156=)	rs149729088
NM_000466.3(PEX1):c.91C>T (p.Leu31=)	rs1585269118

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