List of variants in gene DNAAF3 reported as benign by GeneDx

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001256715.2(DNAAF3):c.86-155G>A	rs3848619	0.37411
NM_001256715.2(DNAAF3):c.323-88G>T	rs7249414	0.24890
NM_001256715.2(DNAAF3):c.481-52C>T	rs3848617	0.24800
NC_000019.10:g.55166857T>A	rs6509927	0.17787
NM_001256715.2(DNAAF3):c.663+44C>A	rs12104158	0.12741
NM_001256715.2(DNAAF3):c.1048+278C>T	rs73066627	0.07533
NM_001256715.2(DNAAF3):c.913-111A>G	rs58218194	0.05702
NM_001256715.2(DNAAF3):c.790-46G>T	rs74380007	0.05612
NM_001256715.2(DNAAF3):c.664-60G>A	rs78584250	0.05598
NM_001256715.2(DNAAF3):c.1048+287T>C	rs77353455	0.05184
NM_001256715.2(DNAAF3):c.322+145C>T	rs7247150	0.01468
NC_000019.10:g.55167031C>A	rs61245087
NC_000019.10:g.55167031del	rs57919151
NM_001256715.2(DNAAF3):c.1048+14_1048+34del	rs6146559
NM_001256715.2(DNAAF3):c.1163+96_1163+132del	rs776965948
NM_001256715.2(DNAAF3):c.1164-116del	rs67301370
NM_001256715.2(DNAAF3):c.912+135A>G	rs59663064

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