List of variants in gene combination LOC129932856, LYST 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000081.4(LYST):c.-131G>C
NM_000081.4(LYST):c.-134G>A
NM_000081.4(LYST):c.-136G>A
NM_000081.4(LYST):c.-139G>A
NM_000081.4(LYST):c.-140G>C
NM_000081.4(LYST):c.-142C>T

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