ClinVar Miner

List of variants in gene combination IL10RA, LOC130006833 reported as likely pathogenic for Inflammatory bowel disease 28

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)
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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NC_000011.10:g.117986319_117986651del	rs2134978631

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