List of variants in gene combination CAPZA1, MOV10, PPM1J, RHOC, ST7L, TAFA3 reported as uncertain significance for adenocarcinoma

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 1p13.2(chr1:113134186-113265713)x3

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