Variants in gene MBD5 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_001378120.1(MBD5):c.1638C>T (p.Ala546=)	rs116413446	0.00337
NM_001378120.1(MBD5):c.2030G>A (p.Ser677Asn)	rs114314967	0.00198
NM_001378120.1(MBD5):c.3978C>T (p.Val1326=)	rs35692977	0.00123
NM_001378120.1(MBD5):c.1368G>T (p.Ser456=)	rs146020786	0.00115
NM_001378120.1(MBD5):c.3754-9T>C	rs370173652	0.00100
NM_001378120.1(MBD5):c.4595G>A (p.Arg1532Gln)	rs35934694	0.00074
NM_001378120.1(MBD5):c.3743A>G (p.Gln1248Arg)	rs143028540	0.00068
NM_001378120.1(MBD5):c.-831+9dup	rs796052705	0.00061
NM_001378120.1(MBD5):c.236G>A (p.Gly79Glu)	rs34995577	0.00061
NM_001378120.1(MBD5):c.1382G>A (p.Arg461His)	rs139964770	0.00042
NM_001378120.1(MBD5):c.2254A>G (p.Ile752Val)	rs147455836	0.00040
NM_001378120.1(MBD5):c.471A>G (p.Thr157=)	rs138433455	0.00040
NM_001378120.1(MBD5):c.4401C>T (p.Val1467=)	rs144957555	0.00038
NM_001378120.1(MBD5):c.3842C>T (p.Thr1281Ile)	rs145475623	0.00034
NM_001378120.1(MBD5):c.4009A>G (p.Ile1337Val)	rs115940994	0.00028
NM_001378120.1(MBD5):c.276A>G (p.Ala92=)	rs141855494	0.00022
NM_001378120.1(MBD5):c.599G>A (p.Arg200Gln)	rs149278000	0.00020
NM_001378120.1(MBD5):c.1111C>G (p.Gln371Glu)	rs536900412	0.00001
NM_001378120.1(MBD5):c.2605G>A (p.Val869Ile)	rs116207524

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