List of variants in gene DNAAF5 reported as likely 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_017802.4(DNAAF5):c.1784-283G>A	rs62432867	0.01845
NM_017802.4(DNAAF5):c.780+167A>G	rs78844251	0.01793
NM_017802.4(DNAAF5):c.2239+144C>T	rs75212015	0.01533
NM_017802.4(DNAAF5):c.1932-307C>T	rs77954069	0.01527
NM_017802.4(DNAAF5):c.1470+168C>T	rs76611410	0.01525
NM_017802.4(DNAAF5):c.781-301A>G	rs77251857	0.01484
NM_017802.4(DNAAF5):c.2432-227G>T	rs116103099	0.01432
NM_017802.4(DNAAF5):c.905+121G>A	rs145951674	0.01391
NM_017802.4(DNAAF5):c.921C>A (p.Ser307Arg)	rs113374052	0.01326
NM_017802.4(DNAAF5):c.1258-66G>A	rs75334176	0.01324
NM_017802.4(DNAAF5):c.781-160G>C	rs77408922	0.01290
NM_017802.4(DNAAF5):c.2432-316C>T	rs78022191	0.01103
NM_017802.4(DNAAF5):c.1470+63A>G	rs114376033	0.00977
NM_017802.4(DNAAF5):c.1784-258A>G	rs185920353	0.00657
NM_017802.4(DNAAF5):c.2431+262G>A	rs116936105	0.00608
NM_017802.4(DNAAF5):c.905+48G>A	rs77140093	0.00495
NM_017802.4(DNAAF5):c.1783+85C>T	rs183215567	0.00365
NM_017802.4(DNAAF5):c.2082+236C>T	rs76962855
NM_017802.4(DNAAF5):c.2432-258_2432-182del	rs2128088284

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