List of variants in gene combination IGHMBP2, LOC126861245 reported as likely benign for not specified

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

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002180.3(IGHMBP2):c.1603A>G (p.Ile535Val)	rs140221316	0.00124
NM_002180.3(IGHMBP2):c.1581C>T (p.Asp527=)	rs149736203	0.00038
NM_002180.3(IGHMBP2):c.1538-20C>T	rs147148090

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