List of variants in gene combination FADD, LOC130006295 reported as likely benign for FADD-related immunodeficiency

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_003824.4(FADD):c.286+20G>A	rs745305568	0.00028
NM_003824.4(FADD):c.264C>A (p.Ala88=)	rs531922348	0.00002
NM_003824.4(FADD):c.286+12G>C	rs1184018545	0.00002
NM_003824.4(FADD):c.286+9G>C	rs1027426173	0.00001
NM_003824.4(FADD):c.258G>A (p.Ala86=)	rs2049439639
NM_003824.4(FADD):c.286+10G>A
NM_003824.4(FADD):c.286+15G>T	rs2497597909
NM_003824.4(FADD):c.286+18_286+24del	rs2497597913
NM_003824.4(FADD):c.286+20G>T
NM_003824.4(FADD):c.286+6_286+10dup
NM_003824.4(FADD):c.286+8C>T	rs1189166661

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