rs373759, C11orf65;ATM

N. diseases: 3
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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.882 0.120 11 108349930 intron variant C/T snv 0.27 0.010 1.000 1 2018 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.882 0.120 11 108349930 intron variant C/T snv 0.27 0.010 1.000 1 2018 2018
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.882 0.120 11 108349930 intron variant C/T snv 0.27 0.010 1.000 1 2014 2014