Related gene-specific medical variations for Gene (Select 10459) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2870086	NM_006341.4(MAD2L2):c.41-6dup	LOC129929411, MAD2L2	Duplication (intron variant)	not provided	GBenign
Select item 2790636	NM_006341.4(MAD2L2):c.41-12G>T	LOC129929411, MAD2L2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2778087	NM_006341.4(MAD2L2):c.41-12G>A	LOC129929411, MAD2L2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2638237	NM_001127325.2(MAD2L2):c.-13+3286G>A	DRAXIN, MAD2L2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2189964	NM_006341.4(MAD2L2):c.41-6C>T	LOC129929411, MAD2L2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2164123	NM_006341.4(MAD2L2):c.41-8C>A	LOC129929411, MAD2L2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2065016	NM_006341.4(MAD2L2):c.41-7C>G	LOC129929411, MAD2L2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1971207	NM_006341.4(MAD2L2):c.41-20C>T	LOC129929411, MAD2L2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 775512	NM_006341.4(MAD2L2):c.41-7C>A	LOC129929411, MAD2L2	Single nucleotide variant (intron variant)	not provided	GBenign

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