List of variants in gene RASGRP2 reported as pathogenic for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001098671.2(RASGRP2):c.1142C>T (p.Ser381Phe)	rs767965347
NM_001098671.2(RASGRP2):c.1479dup (p.Arg494fs)	rs774996406
NM_001098671.2(RASGRP2):c.337C>T (p.Arg113Ter)	rs1592384832
NM_001098671.2(RASGRP2):c.706C>T (p.Gln236Ter)	rs2135780423
NM_001098671.2(RASGRP2):c.742G>T (p.Gly248Trp)	rs587777529

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