Related gene-specific medical variations for Gene (Select 3300) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2440927	NM_006736.6(DNAJB2):c.65+5G>T	DNAJB2	Single nucleotide variant (intron variant)	Neuronopathy, distal hereditary motor, autosomal recessive 5	GUncertain significance
Select item 1330564	NM_006736.6(DNAJB2):c.233C>T (p.Thr78Ile)	DNAJB2 (T78I)	Single nucleotide variant (missense variant)	Neuronopathy, distal hereditary motor, autosomal recessive 5	GUncertain significance
Select item 1188674	NM_006736.6(DNAJB2):c.-37+75C>T	DNAJB2, LOC129935648	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 680749	NM_006736.6(DNAJB2):c.-36-110G>C	DNAJB2, LOC129935648	Single nucleotide variant (intron variant)	Neuronopathy, distal hereditary motor, autosomal recessive 5 +1 more	GBenign
Select item 512511	NM_006736.6(DNAJB2):c.-37+10G>C	DNAJB2, LOC129935648	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 382216	NM_006736.6(DNAJB2):c.-37+20T>G	DNAJB2, LOC129935648	Single nucleotide variant (intron variant)	not specified +1 more	GBenign

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