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: rs9930506
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36
CUI: C0001206
Disease: Acromegaly
Acromegaly 		0.010 1.000 1 2018 2018
dbSNP: rs17817449
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		0.010 1.000 1 2010 2010
dbSNP: rs17817449
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		0.010 1.000 1 2010 2010
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0001430
Disease: Adenoma
Adenoma 		0.020 1.000 2 2011 2012
dbSNP: rs17817449
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv
CUI: C0001430
Disease: Adenoma
Adenoma 		0.010 1.000 1 2011 2011
dbSNP: rs8050136
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40
CUI: C0001430
Disease: Adenoma
Adenoma 		0.010 1.000 1 2011 2011
dbSNP: rs17817449
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		0.010 1.000 1 2011 2011
dbSNP: rs8044769
rs8044769
FTO
0.851 0.200 16 53805223 intron variant T/A;C;G snv
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		0.010 1.000 1 2011 2011
dbSNP: rs8050136
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		0.010 1.000 1 2011 2011
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms 		0.010 1.000 1 2018 2018
dbSNP: rs17817449
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv
CUI: C0085762
Disease: Alcohol abuse
Alcohol abuse 		0.010 1.000 1 2019 2019
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.030 1.000 3 2011 2014
dbSNP: rs12597786
rs12597786
FTO
1.000 0.080 16 53787395 intron variant C/T snv 3.2E-02
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.010 1.000 1 2013 2013
dbSNP: rs17817449
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.010 1.000 1 2013 2013
dbSNP: rs7204609
rs7204609
FTO
0.827 0.200 16 53799693 intron variant T/C snv 0.14
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.010 1.000 1 2013 2013
dbSNP: rs8050136
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.010 1.000 1 2017 2017
dbSNP: rs8062891
rs8062891
FTO ; LOC105371271
1.000 0.080 16 54055160 intron variant T/C snv 0.80
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.010 1.000 1 2013 2013
dbSNP: rs11075996
rs11075996
FTO
1.000 0.080 16 53824112 intron variant C/A;T snv 0.38
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2012 2012
dbSNP: rs11075997
rs11075997
FTO
1.000 0.080 16 53825000 intron variant C/T snv 0.39
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2012 2012
dbSNP: rs6499640
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2012 2012
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2011 2011
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0003125
Disease: Anorexia Nervosa
Anorexia Nervosa 		0.010 1.000 1 2012 2012
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0003507
Disease: Aortic Valve Stenosis
Aortic Valve Stenosis 		0.010 1.000 1 2015 2015
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.020 1.000 2 2011 2015
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2016 2016