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rs786201005(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs786201005
GeneISG15
Chromosome1
Position1,014,143
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of an immunodeficiency mutation
(T;T) 3 Causes a lack of ISG15 which in turn causes basal ganglia calcification, auto-inflammation and susceptibility to mycobacterial disease