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: rs1059362
rs1059362
6 32580773 synonymous variant G/A snv 7.2E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs113399573
rs113399573
6 32591382 upstream gene variant C/T snv 0.23
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs116763083
rs116763083
6 32602155 intergenic variant T/A snv 4.4E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2308765
rs2308765
6 32581757 missense variant A/C;G;T snv 7.6E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2012 2012
dbSNP: rs2647062
rs2647062
6 32602640 intergenic variant A/C snv 0.13
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018
dbSNP: rs2647074
rs2647074
6 32606583 intergenic variant C/T snv 0.30
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 1 2018 2018
dbSNP: rs2647074
rs2647074
6 32606583 intergenic variant C/T snv 0.30
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2760995
rs2760995
6 32606581 intergenic variant G/A snv 0.20
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria
0.700 1.000 1 2019 2019
dbSNP: rs28366255
rs28366255
6 32591705 upstream gene variant C/A;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs28366266
rs28366266
6 32591976 upstream gene variant T/C snv 0.12
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome
0.700 1.000 1 2018 2018
dbSNP: rs9256938
rs9256938
6 32579417 intron variant C/A;G snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs9270493
rs9270493
6 32591333 upstream gene variant T/C snv 0.25
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs9270637
rs9270637
6 32597873 intergenic variant A/C;G snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs9270891
rs9270891
6 32604051 intergenic variant T/G snv 0.60
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 4 2007 2011
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.710 1.000 2 2013 2016
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 1.000 1 2012 2012
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris
0.700 1.000 1 2012 2012
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.700 1.000 1 2013 2013
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2007 2007
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2016 2016
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.010 1.000 1 2016 2016
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections
0.700 1.000 1 2013 2013
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
0.010 1.000 1 2016 2016
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.700 1.000 1 2012 2012