List of variants in gene DNAL1 reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_031427.4(DNAL1):c.*2923dup	rs568527612	0.00091
NM_031427.4(DNAL1):c.6161_6162insCA	rs886050720	0.00025
NM_031427.4(DNAL1):c.*5630del	rs746876867	0.00018
NM_031427.4(DNAL1):c.2600_2604del	rs770668475	0.00011
NM_031427.4(DNAL1):c.22_24del (p.Lys8del)	rs779309893	0.00002
NM_031427.4(DNAL1):c.*1823del	rs59065500
NM_031427.4(DNAL1):c.*1824del	rs886050695
NM_031427.4(DNAL1):c.*2570del	rs746527785
NM_031427.4(DNAL1):c.3110_3111dup	rs769560403
NM_031427.4(DNAL1):c.*334del	rs147394906
NM_031427.4(DNAL1):c.*3356del	rs529762916
NM_031427.4(DNAL1):c.*6137del	rs886050714
NM_031427.4(DNAL1):c.*6138TG[10]	rs10679978
NM_031427.4(DNAL1):c.*6138TG[12]	rs10679978
NM_031427.4(DNAL1):c.*6138TG[14]	rs10679978
NM_031427.4(DNAL1):c.*6138TG[15]	rs10679978
NM_031427.4(DNAL1):c.*6138TG[16]	rs10679978
NM_031427.4(DNAL1):c.6147_6148insCG	rs886050719
NM_031427.4(DNAL1):c.*6216dup	rs779734012
NM_031427.4(DNAL1):c.6341_6343del	rs886050724
NM_031427.4(DNAL1):c.*7017dup	rs367557905
NM_031427.4(DNAL1):c.7414_7419del	rs886050727

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