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: rs3845971
rs3845971
FHIT
1.000 0.080 3 60014946 intron variant T/C snv 0.28
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2007 2007
dbSNP: rs760317
rs760317
FHIT
0.925 0.080 3 60113429 intron variant A/G snv 0.60
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2007 2007
dbSNP: rs760317
rs760317
FHIT
0.925 0.080 3 60113429 intron variant A/G snv 0.60
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2007 2007
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: rs9874888
rs9874888
FHIT
1.000 0.080 3 60030591 intron variant T/A snv 0.30
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
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: 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: 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: 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: 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
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: 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: 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: 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: 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: rs2365389
rs2365389
FHIT
3 61250788 intron variant C/T snv 0.56
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017