C4014584[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1248539	NM_001098671.2(RASGRP2):c.1591+45T>G	RASGRP2	Single nucleotide variant (intron variant)	Platelet-type bleeding disorder 18 +1 more	GBenign
Select item 1289252	NM_001098671.2(RASGRP2):c.1174-43T>C	RASGRP2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1287361	NM_001098671.2(RASGRP2):c.1096-44T>C	RASGRP2	Single nucleotide variant (intron variant)	Platelet-type bleeding disorder 18 +1 more	GBenign
Select item 1231140	NM_001098671.2(RASGRP2):c.523-34A>G	RASGRP2	Single nucleotide variant (intron variant)	Platelet-type bleeding disorder 18 +1 more	GBenign
Select item 1259868	NM_001098671.2(RASGRP2):c.372-45T>G	RASGRP2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

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