List of variants in gene RASGRP2 reported as likely 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001098671.2(RASGRP2):c.1033G>C (p.Ala345Pro)	rs200434813
NM_001098671.2(RASGRP2):c.1479dup (p.Arg494fs)	rs774996406
NM_001098671.2(RASGRP2):c.1480dup (p.Arg494fs)	rs1555122100
NM_001098671.2(RASGRP2):c.1490del (p.Phe497fs)	rs752492512
NM_001098671.2(RASGRP2):c.542T>C (p.Phe181Ser)	rs1060499609
NM_001098671.2(RASGRP2):c.742G>C (p.Gly248Arg)	rs587777529
NM_001098671.2(RASGRP2):c.887G>A (p.Cys296Tyr)	rs2135765010
NM_001098671.2(RASGRP2):c.914G>A (p.Gly305Asp)	rs1592371840

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