Source: BEFREE

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: rs2298383
rs2298383
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders
0.020 1.000 2 2008 2019
dbSNP: rs2236624
rs2236624
0.925 0.200 22 24440056 intron variant T/C snv 0.80
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
0.010 1.000 1 2010 2010
dbSNP: rs2236624
rs2236624
0.925 0.200 22 24440056 intron variant T/C snv 0.80
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
0.010 1.000 1 2011 2011
dbSNP: rs2298383
rs2298383
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv
CUI: C0003467
Disease: Anxiety
Anxiety
0.010 1.000 1 2008 2008
dbSNP: rs2298383
rs2298383
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv
CUI: C0392156
Disease: Akathisia
Akathisia
0.010 1.000 1 2016 2016
dbSNP: rs2298383
rs2298383
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv
CUI: C0917801
Disease: Sleeplessness
Sleeplessness
0.010 1.000 1 2019 2019
dbSNP: rs2298383
rs2298383
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.010 1.000 1 2019 2019
dbSNP: rs2298383
rs2298383
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.010 1.000 1 2019 2019
dbSNP: rs2298383
rs2298383
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv
CUI: C0270612
Disease: Leukoencephalopathy
Leukoencephalopathy
0.010 1.000 1 2016 2016
dbSNP: rs2298383
rs2298383
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv
CUI: C0349217
Disease: Depressive episode, unspecified
Depressive episode, unspecified
0.010 1.000 1 2019 2019
dbSNP: rs2298383
rs2298383
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2017 2017
dbSNP: rs2298383
rs2298383
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv
CUI: C0344315
Disease: Depressed mood
Depressed mood
0.010 1.000 1 2019 2019
dbSNP: rs2298383
rs2298383
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv
CUI: C0236734
Disease: Caffeine related disorders
Caffeine related disorders
0.010 1.000 1 2008 2008
dbSNP: rs3032740
rs3032740
22 24439073 intron variant TTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT delins
CUI: C0236734
Disease: Caffeine related disorders
Caffeine related disorders
0.010 1.000 1 2008 2008
dbSNP: rs35320474
rs35320474
1.000 0.080 22 24441941 3 prime UTR variant -/T delins
CUI: C0003578
Disease: Apnea
Apnea
0.010 1.000 1 2012 2012
dbSNP: rs35320474
rs35320474
1.000 0.080 22 24441941 3 prime UTR variant -/T delins
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia
0.010 1.000 1 2012 2012
dbSNP: rs3761422
rs3761422
1.000 0.040 22 24430704 intron variant T/C snv 0.62
CUI: C0003467
Disease: Anxiety
Anxiety
0.010 < 0.001 1 2010 2010
dbSNP: rs3761422
rs3761422
1.000 0.040 22 24430704 intron variant T/C snv 0.62
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders
0.010 < 0.001 1 2010 2010
dbSNP: rs3761422
rs3761422
1.000 0.040 22 24430704 intron variant T/C snv 0.62
CUI: C0236734
Disease: Caffeine related disorders
Caffeine related disorders
0.010 < 0.001 1 2010 2010
dbSNP: rs3761422
rs3761422
1.000 0.040 22 24430704 intron variant T/C snv 0.62
CUI: C0018681
Disease: Headache
Headache
0.010 < 0.001 1 2010 2010
dbSNP: rs4822489
rs4822489
0.925 0.200 22 24437792 intron variant T/G snv 0.48
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.010 1.000 1 2015 2015
dbSNP: rs4822489
rs4822489
0.925 0.200 22 24437792 intron variant T/G snv 0.48
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
0.010 1.000 1 2011 2011
dbSNP: rs5996696
rs5996696
1.000 0.040 22 24431654 intron variant A/C snv 0.12
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 1.000 1 2011 2011
dbSNP: rs71651683
rs71651683
1.000 0.040 22 24432885 5 prime UTR variant C/T snv 3.6E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 1.000 1 2011 2011
dbSNP: rs9624472
rs9624472
0.925 0.040 22 24438763 splice region variant A/G snv 0.10
CUI: C2747816
Disease: Complicated malaria
Complicated malaria
0.010 1.000 1 2010 2010