ClinVar Miner

List of variants in gene combination BLM, FES, FURIN, HDDC3, MAN2A2, PRC1, RCCD1, UNC45A reported as uncertain significance for Bloom syndrome

Included ClinVar conditions (1):

Bloom syndrome

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: 2

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HGVS	dbSNP	gnomAD frequency
NC_000015.10:g.(?_90782812)_(90968837_?)dup
NC_000015.9:g.(?_91290623)_(91512067_?)dup

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