Variants in gene IGHMBP2 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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_002180.3(IGHMBP2):c.1488C>A (p.Cys496Ter)	rs145226920	0.00016
NM_002180.3(IGHMBP2):c.1478C>T (p.Thr493Ile)	rs780594709	0.00003
NM_002180.3(IGHMBP2):c.1156T>C (p.Trp386Arg)	rs759641927	0.00002
NM_002180.3(IGHMBP2):c.1273C>T (p.Arg425Cys)	rs1303837541	0.00001
NM_002180.3(IGHMBP2):c.1327C>T (p.Arg443Cys)	rs751549678	0.00001
NM_002180.3(IGHMBP2):c.2362C>T (p.Arg788Ter)	rs199839840	0.00001
NM_002180.3(IGHMBP2):c.547+1G>A	rs1057518588	0.00001
NM_002180.3(IGHMBP2):c.2540del (p.Gln847fs)	rs1225532037
NM_002180.3(IGHMBP2):c.2911_2912del (p.Arg971fs)	rs724159994
NM_002180.3(IGHMBP2):c.449+1G>T	rs797044802
NM_002180.3(IGHMBP2):c.638A>G (p.His213Arg)	rs137852666

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