RS1057518733 SMARCD2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Specific granule deficiency 1
Autosomal recessive severe congenital neutropenia
Specific granule deficiency 2
Specific granule deficiency 1
Autosomal recessive severe congenital neutropenia
Specific granule deficiency 2
Other Variants in SMARCD2