ClinVar Miner

List of variants in gene combination ABCC1, ABCC6, BMERB1, CEP20, MARF1, MPV17L, MYH11, NDE1, NOMO3, XYLT1 reported as not provided for partial deletion of the short arm of chromosome 16

Included ClinVar conditions (6):

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: 1

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 16p13.11-12.3(chr16:15494600-18141051)x1

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