Related gene-specific medical variations for Gene (Select 1131) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808867	GRCh37/hg19 1q43(chr1:239786186-239808882)x1	CHRM3	Copy number loss	not provided	GUncertain significance
Select item 1696763	NM_001375978.1(CHRM3):c.-313+2514G>A	CHRM3	Single nucleotide variant (intron variant)	Prune belly syndrome	GUncertain significance
Select item 980421	GRCh37/hg19 1q43(chr1:239367007-239974659)x3	CHRM3	Copy number gain	not provided	GUncertain significance
Select item 814185	GRCh37/hg19 1q43(chr1:239823151-239862101)x1	CHRM3	Copy number loss	not provided	GUncertain significance
Select item 686266	GRCh37/hg19 1q43(chr1:239601103-239965763)x3	CHRM3	Copy number gain	not provided	GUncertain significance
Select item 395530	GRCh37/hg19 1q43(chr1:239678218-239969806)x3	CHRM3	Copy number gain	See cases	GUncertain significance
Select item 156772	NG_032046.2:g.169545_239936dup	CHRM3	Duplication	Gestational diabetes mellitus uncontrolled	Gnot provided

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