List of variants in gene combination IGH, IGHM reported as benign for hematologic disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NC_000014.9:g.105855041A>G	rs10287	0.05231
NC_000014.9:g.105855988G>C	rs113762053	0.04825
NC_000014.9:g.105855203G>A
NC_000014.9:g.105856156C>T	rs201981439

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