rs9930506, FTO

N. diseases: 16
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.
Obesity
CUI: C0028754
Disease: Obesity
1111 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.760 0.857 7 2008 2018
Body mass index
CUI: C1305855
Disease: Body mass index
2689 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.700 1.000 2 2007 2019
Body mass index procedure
CUI: C0005893
Disease: Body mass index procedure
252 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.700 1.000 1 2014 2014
Body Weight
CUI: C0005910
Disease: Body Weight
92 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.700 1.000 1 2007 2007
Finding of body mass index
CUI: C0578022
Disease: Finding of body mass index
252 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.700 1.000 1 2014 2014
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.700 1.000 1 2007 2007
Waist Circumference
CUI: C0455829
Disease: Waist Circumference
183 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.700 1.000 1 2009 2009
Waist-Hip Ratio
CUI: C0205682
Disease: Waist-Hip Ratio
1138 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.700 1.000 1 2007 2007
Acromegaly
CUI: C0001206
Disease: Acromegaly
25 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.010 1.000 1 2018 2018
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.010 1.000 1 2017 2017
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.010 1.000 1 2017 2017
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.010 1.000 1 2011 2011
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.010 1.000 1 2014 2014
Obesity, Morbid
CUI: C0028756
Disease: Obesity, Morbid
49 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.010 1.000 1 2016 2016
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.010 1.000 1 2018 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.010 1.000 1 2014 2014