ClinVar Miner

List of variants in gene combination ADA, LOC107303343 reported as uncertain significance for T-B- severe combined immunodeficiency

Included ClinVar conditions (13):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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NM_000022.4(ADA):c.162G>A (p.Lys54=) rs45557242
NM_000022.4(ADA):c.218+2dup rs1555845122
NM_000022.4(ADA):c.57C>A (p.Asp19Glu)
NM_000022.4(ADA):c.58G>A (p.Gly20Arg) rs121908724
NM_000022.4(ADA):c.61T>G (p.Ser21Ala)

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