rs12325817, PEMT

N. diseases: 7
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 0.807 0.320 17 17583205 intron variant C/A;G;T snv 0.010 1.000 1 2008 2008
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.807 0.320 17 17583205 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.807 0.320 17 17583205 intron variant C/A;G;T snv 0.010 1.000 1 2013 2013
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.807 0.320 17 17583205 intron variant C/A;G;T snv 0.010 1.000 1 2013 2013
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.807 0.320 17 17583205 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.807 0.320 17 17583205 intron variant C/A;G;T snv 0.010 1.000 1 2008 2008
Triglyceride storage disease with ichthyosis
CUI: C0268238
Disease: Triglyceride storage disease with ichthyosis
8 0.807 0.320 17 17583205 intron variant C/A;G;T snv 0.010 1.000 1 2011 2011