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

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_002180.3(IGHMBP2):c.1273C>T (p.Arg425Cys)	rs1303837541	0.00002
NM_002180.3(IGHMBP2):c.1198G>A (p.Asp400Asn)	rs779654686	0.00001
NM_002180.3(IGHMBP2):c.1263C>A (p.Ser421Arg)	rs749343954	0.00001
NM_002180.3(IGHMBP2):c.1523C>T (p.Ser508Leu)	rs754465226
NM_002180.3(IGHMBP2):c.1807C>G (p.Arg603Gly)	rs1465803265
NM_002180.3(IGHMBP2):c.2911_2912del (p.Arg971fs)	rs724159994

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