List of variants in gene DNAAF3 reported as uncertain significance 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001256715.2(DNAAF3):c.323-4del	rs201986299	0.00533
NM_001256715.2(DNAAF3):c.832G>A (p.Ala278Thr)	rs200775946	0.00187
NM_001256714.1(DNAAF3):c.2T>C (p.Met1Thr)	rs200365972	0.00131
NM_001256715.2(DNAAF3):c.1256G>A (p.Arg419Gln)	rs373489149	0.00007
NM_001256715.2(DNAAF3):c.789+1G>C	rs770143722	0.00006
NM_001256715.2(DNAAF3):c.271A>G (p.Met91Val)	rs1181045345	0.00003
NM_001256715.2(DNAAF3):c.1205C>T (p.Ala402Val)	rs764412803	0.00002
NM_001256715.2(DNAAF3):c.1251C>T (p.Asp417=)	rs779990994	0.00002
NM_001256715.2(DNAAF3):c.1354G>C (p.Ala452Pro)
NM_001256715.2(DNAAF3):c.1543G>A (p.Gly515Ser)
NM_001256715.2(DNAAF3):c.678C>A (p.His226Gln)
NM_001256715.2(DNAAF3):c.773G>C (p.Gly258Ala)
NM_001256715.2(DNAAF3):c.86-66T>A

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