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: 14

Download table as spreadsheet

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.1909C>T (p.Arg637Cys)	rs201563456	0.00003
NM_002180.3(IGHMBP2):c.1156T>C (p.Trp386Arg)	rs759641927	0.00002
NM_002180.3(IGHMBP2):c.1273C>T (p.Arg425Cys)	rs1303837541	0.00002
NM_002180.3(IGHMBP2):c.1693G>A (p.Asp565Asn)	rs770111639	0.00002
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.1336C>T (p.Gln446Ter)	rs372181708
NM_002180.3(IGHMBP2):c.1398del (p.Val467fs)	rs2496054182
NM_002180.3(IGHMBP2):c.2540del (p.Gln847fs)	rs1225532037
NM_002180.3(IGHMBP2):c.449+1G>T	rs797044802
NM_002180.3(IGHMBP2):c.638A>G (p.His213Arg)	rs137852666

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.