List of variants in gene IGHMBP2 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_002180.3(IGHMBP2):c.1738G>A (p.Val580Ile)	rs137852667	0.00004
NM_002180.3(IGHMBP2):c.138T>A (p.Cys46Ter)	rs372000714	0.00001
NM_002180.3(IGHMBP2):c.2611+1G>T	rs786205090	0.00001
NM_002180.3(IGHMBP2):c.707T>G (p.Leu236Ter)	rs137852669	0.00001
NC_000011.10:g.(68906754_68906786)_(68925257_68925289)del
NM_002180.3(IGHMBP2):c.1107C>G (p.Phe369Leu)	rs137852670
NM_002180.3(IGHMBP2):c.1118T>G (p.Val373Gly)	rs724159959
NM_002180.3(IGHMBP2):c.121C>T (p.Gln41Ter)	rs137852668
NM_002180.3(IGHMBP2):c.2911_2912del (p.Arg971fs)	rs724159994
NM_002180.3(IGHMBP2):c.449+1G>T	rs797044802
NM_002180.3(IGHMBP2):c.604T>G (p.Phe202Val)	rs724159958
NM_002180.3(IGHMBP2):c.638A>G (p.His213Arg)	rs137852666
NM_002180.3(IGHMBP2):c.675del (p.Glu226fs)	rs786205089

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