Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs755009196
rs755009196
ATM ; C11orf65
0.925 0.160 11 108332024 missense variant C/G snv 1.6E-05 2.1E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.700 0
dbSNP: rs755009196
rs755009196
ATM ; C11orf65
0.925 0.160 11 108332024 missense variant C/G snv 1.6E-05 2.1E-05
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 0
dbSNP: rs755009196
rs755009196
ATM ; C11orf65
0.925 0.160 11 108332024 missense variant C/G snv 1.6E-05 2.1E-05
CUI: C0023448
Disease: Lymphoid leukemia
Lymphoid leukemia 		0.700 0