"GeneDx"[submitter] AND "LOC130057338"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 561817	NM_002755.3(MAP2K1):c.-767A>C	TIPIN, LOC130057338 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 561873	NM_002755.3(MAP2K1):c.-695A>T	LOC130057338, MAP2K1 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign