"Invitae"[submitter] AND "ARHGEF25"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 768558	NM_182947.4(ARHGEF25):c.1517= (p.Gln506=)	ARHGEF25	Variation (no sequence alteration +1 more)	not provided	GBenign
Select item 2425252	NC_000012.11:g.(?_57971476)_(58025915_?)dup	ARHGEF25, B4GALNT1 +3 more	Duplication	Spastic paraplegia	GUncertain significance
Select item 2422308	NC_000012.11:g.(?_57534470)_(58190366_?)dup	AGAP2, ARHGAP9 +27 more	Duplication	Familial melanoma	GUncertain significance
Select item 1410313	NC_000012.11:g.(?_57881874)_(58190366_?)dup	AGAP2, ARHGEF25 +17 more	Duplication	not provided	GUncertain significance

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