Source: INFERRED ×
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.
Ataxia Telangiectasia
CUI: C0004135
Disease: Ataxia Telangiectasia
0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 0.800 1.000 17 1996 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 0.780 0.875 0 1998 2016
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 0.700 1.000 21 1996 2016
Ataxia-Telangiectasia Variant
CUI: C1876175
Disease: Ataxia-Telangiectasia Variant
0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 0.700 0
BREAST CANCER, SUSCEPTIBILITY TO
CUI: C3469522
Disease: BREAST CANCER, SUSCEPTIBILITY TO
0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 0.700 0
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 0.700 0
T-Cell Prolymphocytic Leukemia
CUI: C2363142
Disease: T-Cell Prolymphocytic Leukemia
0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 0.700 0