ClinVar Miner

List of variants in gene combination FUT7, LINC02908 reported as benign for not provided

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_004479.4(FUT7):c.970T>C (p.Tyr324His)	rs199955257	0.00209
NM_004479.4(FUT7):c.745G>A (p.Gly249Ser)	rs201821837	0.00026

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