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: rs1327295035
rs1327295035
1.000 0.200 6 52187730 missense variant A/G snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2008 2008
dbSNP: rs201890924
rs201890924
1.000 0.200 6 52187736 missense variant G/A snv 5.2E-05 2.8E-05
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2008 2008
dbSNP: rs1360218267
rs1360218267
1.000 0.080 6 52187734 synonymous variant C/T snv 4.0E-06
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2011 2011
dbSNP: rs148704956
rs148704956
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms
0.010 1.000 1 2011 2011
dbSNP: rs17878530
rs17878530
1.000 0.080 6 52189247 synonymous variant C/A;T snv 4.0E-06; 8.4E-05
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2011 2011
dbSNP: rs17880588
rs17880588
1.000 0.080 6 52189226 synonymous variant G/A snv 4.5E-03 1.8E-02
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2011 2011
dbSNP: rs1974226
rs1974226
0.827 0.240 6 52190537 3 prime UTR variant C/T snv 0.15
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis
0.010 1.000 1 2011 2011
dbSNP: rs1974226
rs1974226
0.827 0.240 6 52190537 3 prime UTR variant C/T snv 0.15
CUI: C0876973
Disease: Infectious Lung Disorder
Infectious Lung Disorder
0.010 1.000 1 2011 2011
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
0.010 1.000 1 2011 2011
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.010 1.000 1 2011 2011
dbSNP: rs8193037
rs8193037
0.752 0.320 6 52186311 upstream gene variant G/A;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 1.000 1 2011 2011
dbSNP: rs8193037
rs8193037
0.752 0.320 6 52186311 upstream gene variant G/A;T snv
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
0.010 1.000 1 2011 2011
dbSNP: rs8193037
rs8193037
0.752 0.320 6 52186311 upstream gene variant G/A;T snv
CUI: C0340293
Disease: Anterior myocardial infarction
Anterior myocardial infarction
0.010 1.000 1 2011 2011
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2012 2012
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C2242595
Disease: Mucosal atrophy
Mucosal atrophy
0.010 1.000 1 2012 2012
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0013289
Disease: Duodenal Diseases
Duodenal Diseases
0.010 1.000 1 2012 2012
dbSNP: rs2275913
rs2275913
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28
CUI: C0030920
Disease: Peptic Ulcer
Peptic Ulcer
0.010 1.000 1 2012 2012
dbSNP: rs3748067
rs3748067
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2012 2012
dbSNP: rs3748067
rs3748067
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
Secondary malignant neoplasm of lymph node
0.010 1.000 1 2012 2012
dbSNP: rs3748067
rs3748067
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs3819024
rs3819024
0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34
CUI: C1387164
Disease: allergic rhinitis with asthma
allergic rhinitis with asthma
0.010 1.000 1 2012 2012
dbSNP: rs3819024
rs3819024
0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
0.010 1.000 1 2012 2012
dbSNP: rs3819025
rs3819025
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2012 2012
dbSNP: rs3819025
rs3819025
0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.010 1.000 1 2012 2012