List of variants in gene PEX7 reported as benign for bone disorder

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000288.4(PEX7):c.340-71G>A	rs927181	0.98050
NM_000288.4(PEX7):c.*306T>G	rs1050803	0.51106
NM_000288.4(PEX7):c.130+48_130+53dup	rs11283064	0.50803
NM_000288.4(PEX7):c.-56C>T	rs73777751	0.11791
NM_000288.4(PEX7):c.340-103A>G	rs2295592	0.10001
NM_000288.4(PEX7):c.803+105A>C	rs72985582	0.04283
NM_000288.4(PEX7):c.-31G>A	rs115866467	0.02411
NM_000288.4(PEX7):c.257_258insAGT	rs1801001
NM_000288.4(PEX7):c.-65A>T	rs190537612
NM_000288.4(PEX7):c.-95T>C	rs1321471
NM_000288.4(PEX7):c.747+20_747+24del	rs199624608

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