Source: ALL

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: rs2365389
rs2365389
FHIT
3 61250788 intron variant C/T snv 0.56
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 7 2015 2018
dbSNP: rs10428174
rs10428174
FHIT
3 59828322 intron variant G/A snv 0.72
CUI: C0233849
Disease: Personality Traits
Personality Traits 		0.700 1.000 1 2012 2012
dbSNP: rs1079196
rs1079196
FHIT
3 59821052 intron variant G/A snv 0.22
CUI: C0233849
Disease: Personality Traits
Personality Traits 		0.700 1.000 1 2012 2012
dbSNP: rs11922368
rs11922368
FHIT
3 60882566 intron variant T/C snv 0.61
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1916799
rs1916799
FHIT
3 61247301 intron variant G/A;T snv
CUI: C0005910
Disease: Body Weight
Body Weight 		0.700 1.000 1 2017 2017
dbSNP: rs1916799
rs1916799
FHIT
3 61247301 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs1916799
rs1916799
FHIT
3 61247301 intron variant G/A;T snv
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.700 1.000 1 2017 2017
dbSNP: rs1916801
rs1916801
FHIT
3 61201372 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2365389
rs2365389
FHIT
3 61250788 intron variant C/T snv 0.56
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs2365389
rs2365389
FHIT
3 61250788 intron variant C/T snv 0.56
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs3915074
rs3915074
FHIT
3 61219238 intron variant A/T snv 0.24
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs6782531
rs6782531
FHIT
3 61009928 intron variant G/C;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2014 2014
dbSNP: rs6782531
rs6782531
FHIT
3 61009928 intron variant G/C;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2014 2014
dbSNP: rs9833533
rs9833533
FHIT
3 60582520 intron variant G/A snv 8.3E-02
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 1 2017 2017
dbSNP: rs9833533
rs9833533
FHIT
3 60582520 intron variant G/A snv 8.3E-02
CUI: C0024967
Disease: Maximal Voluntary Ventilation
Maximal Voluntary Ventilation 		0.700 1.000 1 2017 2017
dbSNP: rs9825823
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47
CUI: C0011570
Disease: Mental Depression
Mental Depression 		0.010 1.000 1 2017 2017
dbSNP: rs9825823
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.010 1.000 1 2017 2017
dbSNP: rs9825823
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2017 2017
dbSNP: rs9825823
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47
CUI: C0344315
Disease: Depressed mood
Depressed mood 		0.010 1.000 1 2017 2017
dbSNP: rs9825823
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		0.700 1.000 1 2017 2017
dbSNP: rs11920657
rs11920657
FHIT
0.925 0.040 3 59962844 intron variant G/C snv 4.1E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs11920657
rs11920657
FHIT
0.925 0.040 3 59962844 intron variant G/C snv 4.1E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs138741635
rs138741635
FHIT
0.925 0.040 3 60942161 intron variant T/A;G snv
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		0.700 1.000 1 2017 2017
dbSNP: rs138741635
rs138741635
FHIT
0.925 0.040 3 60942161 intron variant T/A;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2017 2017
dbSNP: rs1966136
rs1966136
FHIT
0.925 0.040 3 61167905 intron variant A/C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019