List of variants in gene combination CDR2, EEF2K, MOSMO, PDZD9, POLR3E, SDR42E2, UQCRC2, VWA3A reported as pathogenic for chromosome 16p12.1 deletion syndrome, 520kb

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
GRCh37/hg19 16p12.2(chr16:21964083-22386845)
GRCh37/hg19 16p12.2(chr16:21964695-22376385)x1
GRCh37/hg19 16p12.2(chr16:21976691-22386881)

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