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: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.010 1.000 1 2010 2010
dbSNP: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
0.010 1.000 1 2015 2015
dbSNP: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
0.010 1.000 1 2019 2019
dbSNP: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
0.010 1.000 1 2010 2010
dbSNP: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2008 2008
dbSNP: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.010 1.000 1 2010 2010
dbSNP: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
CUI: C2747816
Disease: Complicated malaria
Complicated malaria
0.010 1.000 1 2015 2015
dbSNP: rs2069727
rs2069727
0.763 0.320 12 68154443 intron variant T/A;C snv
Childhood Acute Lymphoblastic Leukemia
0.010 1.000 1 2010 2010
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0041330
Disease: Tuberculosis, Spinal
Tuberculosis, Spinal
0.010 1.000 1 2017 2017
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0019270
Disease: Hernia
Hernia
0.010 1.000 1 2017 2017
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
0.010 1.000 1 2019 2019
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0030193
Disease: Pain
Pain
0.010 1.000 1 2017 2017
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
0.010 1.000 1 2015 2015
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary
0.010 1.000 1 2017 2017
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.010 1.000 1 2015 2015
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2008 2008
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0014060
Disease: Encephalitis, St. Louis
Encephalitis, St. Louis
0.010 1.000 1 2010 2010
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0150988
Disease: Sclerodactyly
Sclerodactyly
0.010 1.000 1 2019 2019
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C2747816
Disease: Complicated malaria
Complicated malaria
0.010 1.000 1 2015 2015
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0026272
Disease: Mixed Connective Tissue Disease
Mixed Connective Tissue Disease
0.010 1.000 1 2019 2019
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0278147
Disease: Radicular pain
Radicular pain
0.010 1.000 1 2017 2017
dbSNP: rs2069718
rs2069718
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 1.000 1 2010 2010
dbSNP: rs1861493
rs1861493
0.851 0.280 12 68157416 intron variant G/A snv 0.76
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2008 2008
dbSNP: rs1861493
rs1861493
0.851 0.280 12 68157416 intron variant G/A snv 0.76
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
AURAL ATRESIA, CONGENITAL
0.010 1.000 1 2016 2016