Related gene-specific medical variations for Gene (Select 3507) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2688319	NC_000014.9:g.105852108C>T	IGH, IGHM	Single nucleotide variant	not specified	GBenign
Select item 2688227	NC_000014.9:g.105855558C>T	IGH, IGHM	Single nucleotide variant	not specified	GBenign
Select item 2688004	NC_000014.9:g.105852010C>T	IGH, IGHM	Single nucleotide variant	not specified	GBenign
Select item 2687990	NC_000014.9:g.105855808A>G	IGH, IGHM	Single nucleotide variant	not specified	GBenign
Select item 2428589	NC_000014.9:g.105855203G>A	IGH, IGHM	Single nucleotide variant	Autosomal recessive agammaglobulinemia 1	GBenign
Select item 1339539	NC_000014.9:g.105856013G>T	IGH, IGHM	Single nucleotide variant	Autosomal recessive agammaglobulinemia 1	GLikely pathogenic
Select item 973583	NC_000014.9:g.105855132dup	IGH, IGHM	Duplication	Autosomal recessive agammaglobulinemia 1	GLikely pathogenic
Select item 811340	NC_000014.9:g.105854900G>T	IGH, IGHM	Single nucleotide variant	Autosomal recessive agammaglobulinemia 1	GLikely benign
Select item 810941	NC_000014.9:g.105855041A>G	IGH, IGHM	Single nucleotide variant	Autosomal recessive agammaglobulinemia 1	GBenign
Select item 439815	NC_000014.9:g.105856156C>T	IGHM, IGH	Single nucleotide variant	not provided +1 more	GBenign
Select item 439814	NC_000014.9:g.105855988G>C	IGH, IGHM	Single nucleotide variant	Autosomal recessive agammaglobulinemia 1	GBenign
Select item 427234	NC_000014.9:g.105856087G>A	IGH, IGHM	Single nucleotide variant	Autosomal recessive agammaglobulinemia 1	GPathogenic
Select item 156278	NC_000014.9:g.105854468A>C	IGH, IGHM	Single nucleotide variant	Autosomal recessive agammaglobulinemia 1	GPathogenic
Select item 14813	NC_000014.9:g.105855107C>T	IGH, IGHM	Single nucleotide variant	Autosomal recessive agammaglobulinemia 1	GPathogenic
Select item 14812	NC_000014.9:g.105855623_105855624del	IGH, IGHM	Deletion	Autosomal recessive agammaglobulinemia 1	GPathogenic
Select item 14810	NC_000014.9:g.105854405C>T	IGH, IGHM	Single nucleotide variant	Autosomal recessive agammaglobulinemia 1	GPathogenic
Select item 14809	IGHM, 75-KB DEL	IGHM	Deletion	Autosomal recessive agammaglobulinemia 1	GPathogenic