ClinVar Miner

List of variants in gene SLC7A7 reported as pathogenic by Revvity Omics, Revvity

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003982.4(SLC7A7):c.625+1G>A	rs386833822	0.00004
NM_003982.4(SLC7A7):c.499+1G>A	rs386833817

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