Variants in gene A2ML1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 11

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HGVS	dbSNP	gnomAD frequency
NM_144670.6(A2ML1):c.4061+1G>A	rs202067416	0.00108
NM_144670.6(A2ML1):c.174_175dup (p.Lys59fs)	rs745711489	0.00051
NM_144670.6(A2ML1):c.3967A>C (p.Asn1323His)	rs200176373	0.00043
NM_144670.6(A2ML1):c.814C>T (p.Arg272Trp)	rs201215628	0.00026
NM_144670.6(A2ML1):c.887T>C (p.Val296Ala)	rs192888493	0.00019
NM_144670.6(A2ML1):c.2405G>A (p.Arg802His)	rs201562272	0.00013
NM_144670.6(A2ML1):c.1970G>A (p.Arg657His)	rs372629661	0.00005
NM_144670.6(A2ML1):c.3264+5G>A	rs200006435	0.00001
NM_144670.6(A2ML1):c.483+6C>T	rs754169968	0.00001
NM_144670.6(A2ML1):c.2145del (p.Phe715fs)	rs759217676
NM_144670.6(A2ML1):c.2719_2720del (p.Gly907fs)	rs560609581

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