List of variants in gene PEX2 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000318.3(PEX2):c.*1194A>G	rs4311633	0.98172
NM_000318.3(PEX2):c.*2377A>G	rs4388434	0.94963
NM_000318.3(PEX2):c.*727T>C	rs4610720	0.94956
NM_000318.3(PEX2):c.*2663T>A	rs28435921	0.50526
NM_000318.3(PEX2):c.-164C>A	rs12718	0.21609
NM_000318.3(PEX2):c.*1141G>A	rs10108054	0.03721
NM_000318.3(PEX2):c.*1909G>T	rs112352942	0.03714
NM_000318.3(PEX2):c.*2446C>T	rs73242165	0.03710
NM_000318.3(PEX2):c.24G>A (p.Ala8=)	rs9298285	0.03660
NM_000318.3(PEX2):c.*2338C>T	rs56231626	0.03506
NM_000318.3(PEX2):c.*2142A>G	rs79700176	0.03415
NM_000318.3(PEX2):c.*1696C>T	rs112199677	0.03286
NM_000318.3(PEX2):c.733G>A (p.Ala245Thr)	rs112108739	0.02536
NM_000318.3(PEX2):c.*458G>A	rs143201132	0.02392
NM_000318.3(PEX2):c.*1601T>A	rs116949534	0.01081
NM_000318.3(PEX2):c.*1242A>G	rs73691481	0.01024
NM_000318.3(PEX2):c.*2306A>G	rs59296540	0.01019
NM_000318.3(PEX2):c.*2554G>A	rs116215385	0.01018

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