RS1057517845 WAS

Health Risk Chr X:48688097
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What This Variant Does
"CLNSIG=5
Associated Conditions
X-linked severe congenital neutropenia
Wiskott-Aldrich syndrome
Thrombocytopenia 1
Inborn genetic diseases
Colon adenocarcinoma
X-linked severe congenital neutropenia
Wiskott-Aldrich syndrome
Thrombocytopenia 1
Inborn genetic diseases
Colon adenocarcinoma
Other Variants in WAS
rs2147262829 rs132630268 rs132630269 rs132630270 rs2519281397 rs132630271 rs587776742 rs587776743 rs132630272 rs132630273
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