rs387906717, WAS

N. diseases: 6
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Neutropenia, Severe Congenital, X-Linked
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
14 0.827 0.120 X 48688403 missense variant T/C snv 0.700 0
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.827 0.120 X 48688403 missense variant T/C snv 0.010 1.000 1 2009 2009
Myelodysplasia
CUI: C0026985
Disease: Myelodysplasia
4 0.827 0.120 X 48688403 missense variant T/C snv 0.010 1.000 1 2010 2010
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.827 0.120 X 48688403 missense variant T/C snv 0.010 1.000 1 2010 2010
Neutropenia
CUI: C0027947
Disease: Neutropenia
97 0.827 0.120 X 48688403 missense variant T/C snv 0.010 1.000 1 2009 2009
Wiskott-Aldrich Syndrome
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
34 0.827 0.120 X 48688403 missense variant T/C snv 0.010 1.000 1 2009 2009