ClinVar Miner

List of variants in gene GREM1 reported as benign for Familial colorectal cancer

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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: 2

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HGVS	dbSNP	gnomAD frequency
NM_013372.7(GREM1):c.-2+2140A>G	rs73376930	0.24752
NM_013372.7(GREM1):c.103C>G (p.Pro35Ala)	rs111262341	0.00259

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