Variants in gene ADA with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

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HGVS	dbSNP	gnomAD frequency
NM_000022.4(ADA):c.226C>T (p.Arg76Trp)	rs121908736	0.00081
NM_000022.4(ADA):c.643G>A (p.Ala215Thr)	rs114025668	0.00030
NM_000022.4(ADA):c.821C>T (p.Pro274Leu)	rs121908738	0.00007
NM_000022.4(ADA):c.446G>A (p.Arg149Gln)	rs121908737	0.00006
NM_000022.4(ADA):c.890C>A (p.Pro297Gln)	rs121908718	0.00003
NM_000022.4(ADA):c.454C>A (p.Leu152Met)	rs121908728	0.00002
NM_000022.4(ADA):c.301C>T (p.Arg101Trp)	rs121908717	0.00001
NM_000022.4(ADA):c.631C>T (p.Arg211Cys)	rs121908740	0.00001
NM_000022.4(ADA):c.845G>A (p.Arg282Gln)	rs751635016	0.00001
NM_000022.4(ADA):c.467G>T (p.Arg156Leu)	rs121908722
NM_000022.4(ADA):c.478+6T>A	rs1555844600
NM_000022.4(ADA):c.698C>T (p.Thr233Ile)	rs121908729
NM_000022.4(ADA):c.716G>A (p.Gly239Asp)	rs1312320956

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