LOC101928988[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154848	GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3	LOC130057927, LOC130057928 +1764 more	Copy number gain	See cases	GPathogenic
Select item 787680	NM_014326.5(DAPK2):c.632+8G>T	DAPK2, LOC101928988	Single nucleotide variant	not provided	GBenign/Likely benign
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

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