rs16867253, GRHL1

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.
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 0.700 1.000 1 2016 2016
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 0.700 1.000 1 2016 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 0.700 1.000 1 2016 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 0.700 1.000 1 2016 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 0.700 1.000 1 2016 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 0.700 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 0.700 1.000 1 2016 2016