Related gene-specific medical variations for Gene (Select 23604) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3270873	NM_014326.5(DAPK2):c.628A>G (p.Met210Val)	DAPK2, LOC101928988 (M1V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3080082	NM_014326.5(DAPK2):c.377C>T (p.Ala126Val)	DAPK2, LOC125078101 (A126V)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2491429	NM_014326.5(DAPK2):c.451A>C (p.Lys151Gln)	DAPK2, LOC125078101 (K151Q)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2462210	NM_014326.5(DAPK2):c.405T>G (p.Asp135Glu)	DAPK2, LOC125078101 (D135E)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2386030	NM_014326.5(DAPK2):c.337G>A (p.Asp113Asn)	DAPK2, LOC125078101 (D113N)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2355239	NM_014326.5(DAPK2):c.424A>C (p.Thr142Pro)	DAPK2, LOC125078101 (T142P)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 787680	NM_014326.5(DAPK2):c.632+8G>T	DAPK2, LOC101928988	Single nucleotide variant	not provided	GBenign/Likely benign

ClinVar