RS397514671 STIM1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Combined immunodeficiency due to STIM1 deficiency
Stormorken syndrome
Myopathy with tubular aggregates
Combined immunodeficiency due to STIM1 deficiency
Stormorken syndrome
Myopathy with tubular aggregates
Other Variants in STIM1