ClinVar Miner

List of variants in gene CNIH3, CNIH4, LOC112577544, LOC129932585, LOC129932586, LOC129932587, LOC129932588, LOC129932589, LOC129932590, LOC129932591, LOC129932592, MIR4742, NVL, WDR26 studied for Skraban-Deardorff syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
GRCh38/hg38 1q42.11-42.12(chr1:224304638-224434886)x1

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