rs2292239, ERBB3

N. diseases: 13
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.
Diabetes Mellitus, Insulin-Dependent
954 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.830 1.000 7 2007 2019
Adult type dermatomyositis
CUI: C0221056
Disease: Adult type dermatomyositis
31 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.010 1.000 1 2015 2015
Alopecia Areata
CUI: C0002171
Disease: Alopecia Areata
54 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.700 1.000 1 2015 2015
Autoantibody measurement
CUI: C1272321
Disease: Autoantibody measurement
52 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.700 1.000 1 2011 2011
Dermatomyositis
CUI: C0011633
Disease: Dermatomyositis
34 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.010 1.000 1 2015 2015
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.010 1.000 1 2015 2015
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.010 1.000 1 2015 2015
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.700 1.000 1 2011 2011
MYOTONIC DYSTROPHY 1
CUI: C3250443
Disease: MYOTONIC DYSTROPHY 1
14 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.010 1.000 1 2015 2015
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
37 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.010 1.000 1 2015 2015
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.700 1.000 1 2012 2012
Polymyositis
CUI: C0085655
Disease: Polymyositis
22 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.010 1.000 1 2015 2015
Proliferative diabetic retinopathy
CUI: C0154830
Disease: Proliferative diabetic retinopathy
45 0.742 0.480 12 56088396 intron variant T/G snv 0.65 0.010 1.000 1 2015 2015