List of variants in gene FASLG reported as pathogenic for autoimmune disease

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000639.3(FASLG):c.343C>T (p.Arg115Ter)	rs773045347
NM_000639.3(FASLG):c.44del (p.Val15fs)
NM_000639.3(FASLG):c.473_556del (p.Met158_Glu185del)	rs80358236

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