Source: GWASCAT

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: rs1353545
rs1353545
FHIT
1.000 0.040 3 60302116 intron variant G/C snv 0.36
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 4 2015 2019
dbSNP: rs10222378
rs10222378
FHIT
1.000 0.040 3 61063307 intron variant A/G;T snv 0.55
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		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: 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: rs13061562
rs13061562
FHIT
1.000 0.040 3 61065916 intron variant T/C snv 0.45
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1353545
rs1353545
FHIT
1.000 0.040 3 60302116 intron variant G/C snv 0.36
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
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: 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: rs141954845
rs141954845
FHIT
1.000 0.040 3 61207237 intron variant G/A snv 0.43
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2019 2019
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: 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: 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: 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: 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: 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
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: rs633798
rs633798
FHIT ; LOC105377113
1.000 0.040 3 59876145 intron variant T/C snv 0.41
CUI: C1863416
Disease: Autosomal dominant compelling helio ophthalmic outburst syndrome
Autosomal dominant compelling helio ophthalmic outburst syndrome 		0.700 1.000 1 2016 2016