List of variants in gene combination GGCX, LOC129934217 reported as uncertain significance for hematologic disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000821.7(GGCX):c.-46C>T	rs376371398	0.00130
NM_000821.7(GGCX):c.-53C>T	rs886056381	0.00001
NM_000821.7(GGCX):c.-46C>G	rs376371398

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