ClinVar for MedGen (Select 346679) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065363	NM_004145.4(MYO9B):c.6016G>A (p.Glu2006Lys)	MYO9B (E2006K)	Single nucleotide variant (missense variant)	Celiac disease, susceptibility to, 4	GUncertain significance
Select item 781444	NM_004145.4(MYO9B):c.167G>A (p.Arg56Gln)	MYO9B (R56Q)	Single nucleotide variant (missense variant)	Celiac disease, susceptibility to, 4 +1 more	GBenign/Likely benign
Select item 7521	NM_004145.4(MYO9B):c.4879-123G>A	MYO9B	Single nucleotide variant (intron variant)	Celiac disease, susceptibility to, 4	GBenign

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