Source: BEFREE

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: rs10501920
rs10501920
CNTN5
0.882 0.080 11 99622442 intron variant C/G snv 0.14
CUI: C0018801
Disease: Heart failure
Heart failure 		0.010 1.000 1 2007 2007
dbSNP: rs10501920
rs10501920
CNTN5
0.882 0.080 11 99622442 intron variant C/G snv 0.14
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.010 1.000 1 2007 2007
dbSNP: rs10501920
rs10501920
CNTN5
0.882 0.080 11 99622442 intron variant C/G snv 0.14
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.010 1.000 1 2007 2007
dbSNP: rs1813443
rs1813443
CNTN5
1.000 0.040 11 100140279 intron variant G/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2014 2014
dbSNP: rs6590474
rs6590474
CNTN5
1.000 0.040 11 99982441 intron variant A/C snv 0.71
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa 		0.010 1.000 1 2009 2009
dbSNP: rs737582
rs737582
CNTN5
1.000 0.040 11 99992669 intron variant G/A snv 0.39
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa 		0.010 1.000 1 2009 2009
dbSNP: rs7947224
rs7947224
CNTN5
1.000 0.040 11 100002678 intron variant T/C snv 0.39
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa 		0.010 1.000 1 2009 2009