Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2854275
rs2854275
0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections
Infections 0.800 1.000 1 2013 2013
dbSNP: rs9274407
rs9274407
0.925 0.120 6 32665055 missense variant A/C;T snv 0.77
Chemical and Drug Induced Liver Injury
Digestive System Diseases; Chemically-Induced Disorders 0.800 1.000 1 2011 2011
dbSNP: rs1770
rs1770
1.000 0.120 6 32660056 splice region variant A/G snv 0.31
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.710 1.000 1 2019 2019
dbSNP: rs1063355
rs1063355
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 2 2007 2009
dbSNP: rs1063348
rs1063348
1.000 0.080 6 32660146 3 prime UTR variant A/G snv 0.43
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1063355
rs1063355
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1063355
rs1063355
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs114544105
rs114544105
6 32667852 intron variant G/A snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2017 2017
dbSNP: rs142471762
rs142471762
6 32663606 non coding transcript exon variant TAGGATAT/- delins 6.2E-04
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement
0.700 1.000 1 2017 2017
dbSNP: rs201043192
rs201043192
6 32660761 intron variant GG/- del
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2015 2015
dbSNP: rs201184533
rs201184533
1.000 0.080 6 32665110 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs201386475
rs201386475
1.000 0.120 6 32668286 5 prime UTR variant -/CA delins
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2515895
rs2515895
1.000 0.040 6 32661183 intron variant T/C snv 0.24
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
Hemic and Lymphatic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs281862010
rs281862010
6 32665113 intron variant C/A;G snv 1.5E-05
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2854272
rs2854272
1.000 0.040 6 32661903 non coding transcript exon variant A/G snv 0.38
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
Hemic and Lymphatic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2854275
rs2854275
0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2854275
rs2854275
0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs2854275
rs2854275
0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02
CUI: C0201278
Disease: Antibody measurement (procedure)
Antibody measurement (procedure)
0.700 1.000 1 2013 2013
dbSNP: rs2854277
rs2854277
6 32660307 intron variant C/T snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2018 2018
dbSNP: rs28724231
rs28724231
1.000 0.080 6 32659314 upstream gene variant A/G snv 2.9E-02
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic
Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.700 1.000 1 2019 2019
dbSNP: rs3189152
rs3189152
1.000 0.080 6 32666564 missense variant A/G;T snv 0.19 0.39
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs3828800
rs3828800
1.000 0.120 6 32668286 5 prime UTR variant G/A snv 0.20
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs3828805
rs3828805
0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv
Malignant neoplasm of floor of mouth
Neoplasms; Stomatognathic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs3828805
rs3828805
0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv
Malignant neoplasm of lateral floor of mouth
Neoplasms; Stomatognathic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs3828805
rs3828805
0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv
Malignant neoplasm of anterior portion of floor of mouth
Neoplasms; Stomatognathic Diseases 0.700 1.000 1 2016 2016