rs1800692, TNFRSF1A

N. diseases: 5
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.
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.925 0.120 12 6333180 missense variant A/G snv 0.64 0.71 0.700 1.000 1 2019 2019
ATRIAL SEPTAL DEFECT 1
CUI: C1862389
Disease: ATRIAL SEPTAL DEFECT 1
16 0.925 0.120 12 6333180 missense variant A/G snv 0.64 0.71 0.010 1.000 1 2013 2013
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
96 0.925 0.120 12 6333180 missense variant A/G snv 0.64 0.71 0.010 1.000 1 2013 2013
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.925 0.120 12 6333180 missense variant A/G snv 0.64 0.71 0.010 1.000 1 2013 2013
Fever
CUI: C0015967
Disease: Fever
66 0.925 0.120 12 6333180 missense variant A/G snv 0.64 0.71 0.010 1.000 1 2014 2014