ClinVar Miner

List of variants in gene combination IFNAR1, IFNGR2, IL10RB, TMEM50B reported as uncertain significance for autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NC_000021.8:g.(?_34638751)_(34809289_?)dup

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