List of variants in gene PEX14 reported as benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_004565.3(PEX14):c.384+181T>C	rs284236	0.99593
NM_004565.3(PEX14):c.169+34A>G	rs2480779	0.95850
NM_004565.3(PEX14):c.169+176A>G	rs2480778	0.94426
NM_004565.3(PEX14):c.37-74C>T	rs622623	0.63618
NM_004565.3(PEX14):c.156C>T (p.Phe52=)	rs12375	0.25602
NM_004565.3(PEX14):c.384+14A>T	rs284238	0.19360
NM_004565.3(PEX14):c.384+136G>A	rs284237	0.19304
NM_004565.3(PEX14):c.169+268G>A	rs10779738	0.15823
NM_004565.3(PEX14):c.169+270C>T	rs10864461	0.15812
NM_004565.3(PEX14):c.1032G>T (p.Gly344=)	rs11539794	0.13336
NC_000001.11:g.10474698C>A	rs72869122	0.07162
NM_004565.3(PEX14):c.385-219C>T	rs75827648	0.05080
NM_004565.3(PEX14):c.487+64C>T	rs2242289	0.04366
NM_004565.3(PEX14):c.1014C>T (p.Asp338=)	rs2128414	0.04291
NM_004565.3(PEX14):c.475G>A (p.Val159Met)	rs74052157	0.02375
NM_004565.3(PEX14):c.384+257C>T	rs77256719	0.01733
NM_004565.3(PEX14):c.586-153C>T	rs188386819	0.00671
NC_000001.11:g.10474780C>G	rs115474604
NM_004565.3(PEX14):c.85-248C>T	rs2506889

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