ClinVar Miner

List of variants in gene FASLG reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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_000639.3(FASLG):c.451+7A>G	rs201525996	0.00210
NM_000639.3(FASLG):c.280T>G (p.Leu94Val)	rs56302117	0.00033

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