List of variants in gene RASGRP2 reported as benign for blood coagulation disease

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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.1096-44T>C	rs556356	0.96381
NM_001098671.2(RASGRP2):c.372-45T>G	rs547280	0.91242
NM_001098671.2(RASGRP2):c.523-34A>G	rs550930	0.91216
NM_001098671.2(RASGRP2):c.1174-43T>C	rs553618	0.91127
NM_001098671.2(RASGRP2):c.1591+45T>G	rs533515	0.72151

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