Source: CURATED

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: rs1800682
rs1800682
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs1926203
rs1926203
0.882 0.160 10 88967577 intron variant C/A snv 0.59
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 1 2010 2010
dbSNP: rs1926203
rs1926203
0.882 0.160 10 88967577 intron variant C/A snv 0.59
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.700 1.000 1 2009 2009
dbSNP: rs1926203
rs1926203
0.882 0.160 10 88967577 intron variant C/A snv 0.59
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.700 1.000 1 2009 2009
dbSNP: rs6586163
rs6586163
0.925 0.120 10 88992261 non coding transcript exon variant A/C snv 0.58
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.700 1.000 1 2017 2017
dbSNP: rs6586163
rs6586163
0.925 0.120 10 88992261 non coding transcript exon variant A/C snv 0.58
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma
0.700 1.000 1 2017 2017
dbSNP: rs121434526
rs121434526
0.882 0.120 10 88941794 missense variant G/A snv 7.0E-06
Familial thoracic aortic aneurysm and aortic dissection
0.700 0
dbSNP: rs121434526
rs121434526
0.882 0.120 10 88941794 missense variant G/A snv 7.0E-06
Aortic Aneurysm, Familial Thoracic 2
0.700 0
dbSNP: rs121434527
rs121434527
0.925 0.120 10 88939542 missense variant C/T snv
CUI: C3279690
Disease: MOYAMOYA DISEASE 5
MOYAMOYA DISEASE 5
0.700 0
dbSNP: rs121434528
rs121434528
0.925 0.120 10 88939543 missense variant G/A snv 7.0E-06
CUI: C3279690
Disease: MOYAMOYA DISEASE 5
MOYAMOYA DISEASE 5
0.700 0
dbSNP: rs2234767
rs2234767
0.649 0.280 10 88989499 intron variant G/A;T snv 0.15
CUI: C2674950
Disease: LUNG CANCER, SUSCEPTIBILITY TO
LUNG CANCER, SUSCEPTIBILITY TO
0.700 0
dbSNP: rs387906592
rs387906592
0.752 0.280 10 88941309 missense variant C/T snv
CUI: C0009782
Disease: Connective Tissue Diseases
Connective Tissue Diseases
0.700 0
dbSNP: rs397515325
rs397515325
1.000 0.120 10 88947371 missense variant T/C snv
Aortic Aneurysm, Familial Thoracic 6
0.700 0
dbSNP: rs727502878
rs727502878
0.925 0.120 10 88939595 missense variant C/G snv
Aortic Aneurysm, Familial Thoracic 6
0.700 0
dbSNP: rs727502878
rs727502878
0.925 0.120 10 88939595 missense variant C/G snv
Familial thoracic aortic aneurysm and aortic dissection
0.700 0
dbSNP: rs746972765
rs746972765
1.000 10 88941252 missense variant C/T snv
Familial thoracic aortic aneurysm and aortic dissection
0.700 0
dbSNP: rs751300489
rs751300489
1.000 0.120 10 88941836 missense variant A/G snv 2.0E-05 2.8E-05
Aortic Aneurysm, Familial Thoracic 6
0.700 0
dbSNP: rs794728021
rs794728021
0.925 0.120 10 88948815 missense variant C/T snv
Familial thoracic aortic aneurysm and aortic dissection
0.700 0