Variants in gene BTD 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001370658.1(BTD):c.1111C>T (p.Pro371Ser)	rs35034250	0.01555
NM_001370658.1(BTD):c.820A>G (p.Ile274Val)	rs35976361	0.01187
NM_001370658.1(BTD):c.1224C>T (p.Tyr408=)	rs35145938	0.01185
NM_001370658.1(BTD):c.73G>A (p.Gly25Arg)	rs34885143	0.01036
NM_001370658.1(BTD):c.142A>G (p.Ile48Val)	rs114092911	0.00722
NM_001370658.1(BTD):c.202C>G (p.Gln68Glu)	rs151071780	0.00167
NM_001370658.1(BTD):c.201C>T (p.Asn67=)	rs147057169	0.00156
NM_001370658.1(BTD):c.1041C>T (p.Gly347=)	rs142421934	0.00086
NM_001370658.1(BTD):c.152T>C (p.Leu51Pro)	rs397514333

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