List of variants in gene combination CDH10, CDH12, LINC02899, PRDM9 reported as uncertain significance for nutritional 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: 1

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 5p14.3-14.2(chr5:22308420-24492723)

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