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: 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: 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: rs1965143
rs1965143
FHIT
1.000 0.040 3 61062993 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		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
dbSNP: rs1966136
rs1966136
FHIT
0.925 0.040 3 61167905 intron variant A/C;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2019 2019
dbSNP: rs3772475
rs3772475
FHIT
1.000 0.040 3 59970823 intron variant C/A;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.010 1.000 1 2017 2017
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: rs9855931
rs9855931
FHIT
1.000 0.040 3 61063887 intron variant C/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs9869954
rs9869954
FHIT
1.000 0.040 3 61062586 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs139239158
rs139239158
FHIT
1.000 0.080 3 59918603 intron variant C/G snv 1.4E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2020 2020
dbSNP: rs1554600
rs1554600
FHIT
1.000 0.080 3 61172101 intron variant G/C snv 1.8E-02
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.700 1.000 1 2018 2018
dbSNP: rs7612462
rs7612462
FHIT
1.000 0.080 3 61185014 intron variant G/A snv 4.0E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2014 2014
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: 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: rs11130760
rs11130760
FHIT
1.000 0.080 3 60210809 intron variant G/T snv 0.12
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth 		0.010 1.000 1 2017 2017
dbSNP: rs11130760
rs11130760
FHIT
1.000 0.080 3 60210809 intron variant G/T snv 0.12
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma 		0.710 1.000 1 2017 2017
dbSNP: rs17257269
rs17257269
FHIT
1.000 0.080 3 60039779 intron variant T/C snv 0.15
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
dbSNP: rs2366964
rs2366964
FHIT
1.000 0.080 3 59944946 intron variant A/G snv 0.16
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
Secondary malignant neoplasm of colon and/or rectum 		0.700 1.000 1 2019 2019