List of variants in gene IGHMBP2 reported as uncertain significance by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_002180.3(IGHMBP2):c.1064C>T (p.Ala355Val)	rs142062146	0.00231
NM_002180.3(IGHMBP2):c.1193C>T (p.Ala398Val)	rs35193202	0.00187
NM_002180.3(IGHMBP2):c.2922T>G (p.Asp974Glu)	rs147674615	0.00144
NM_002180.3(IGHMBP2):c.2844G>A (p.Gly948=)	rs147918962	0.00105
NM_002180.3(IGHMBP2):c.2793C>T (p.Gly931=)	rs139926138	0.00096
NM_002180.3(IGHMBP2):c.1060+8G>T	rs201147313	0.00076
NM_002180.3(IGHMBP2):c.2176G>A (p.Val726Met)	rs143986510	0.00049
NM_002180.3(IGHMBP2):c.832C>G (p.His278Asp)	rs144681826	0.00044
NM_002180.3(IGHMBP2):c.855G>A (p.Ala285=)	rs147409148	0.00029
NM_002180.3(IGHMBP2):c.2618C>T (p.Pro873Leu)	rs141903179	0.00022
NM_002180.3(IGHMBP2):c.2090C>T (p.Pro697Leu)	rs77807333	0.00006
NM_002180.3(IGHMBP2):c.2643G>A (p.Glu881=)	rs374950193	0.00005
NM_002180.3(IGHMBP2):c.1737C>T (p.Phe579=)	rs368775789	0.00004
NM_002180.3(IGHMBP2):c.808C>T (p.Arg270Cys)	rs201054207	0.00003
NM_002180.3(IGHMBP2):c.1106T>A (p.Phe369Tyr)	rs756791529	0.00001
NM_002180.3(IGHMBP2):c.2796C>T (p.Cys932=)	rs112870015	0.00001
NM_002180.3(IGHMBP2):c.1398C>T (p.Ser466=)	rs147477786
NM_002180.3(IGHMBP2):c.229G>C (p.Ala77Pro)	rs778774954
NM_002180.3(IGHMBP2):c.2458A>G (p.Arg820Gly)	rs1566447241
NM_002180.3(IGHMBP2):c.2818G>A (p.Ala940Thr)	rs757839224
NM_002180.3(IGHMBP2):c.2868C>T (p.Thr956=)	rs752024072

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