List of variants in gene DNAAF3 reported as likely benign for not provided

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001256715.2(DNAAF3):c.1048+202_1048+206dup	rs139659116	0.02383
NC_000019.10:g.55166933T>C	rs8109629	0.01325
NM_001256715.1(DNAAF3):c.-174C>T	rs73066642	0.01124
NM_001256715.2(DNAAF3):c.323-17T>G	rs10407660	0.01106
NM_001256715.2(DNAAF3):c.6C>T (p.Thr2=)	rs150362958	0.00844
NM_001256715.2(DNAAF3):c.913-64A>C	rs368878245	0.00479
NM_001256715.2(DNAAF3):c.913-13C>T	rs146442289	0.00272
NM_001256715.2(DNAAF3):c.832G>A (p.Ala278Thr)	rs200775946	0.00187
NM_001256715.2(DNAAF3):c.1413C>T (p.Pro471=)	rs377325487	0.00033
NM_001256715.2(DNAAF3):c.323-5C>T	rs549295806	0.00013
NM_001256715.2(DNAAF3):c.-92T>G	rs780864867	0.00002
NM_001256715.2(DNAAF3):c.1062G>C (p.Pro354=)
NM_001256715.2(DNAAF3):c.363G>T (p.Leu121=)	rs551100219
NM_001256715.2(DNAAF3):c.708A>G (p.Thr236=)	rs1253487279

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