Source: GWASCAT

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: 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
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
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
0.710 1.000 1 2019 2019
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
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
0.700 1.000 1 2018 2018
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
0.700 1.000 1 2019 2019
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: rs2854275
rs2854275
0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02
CUI: C0004096
Disease: Asthma
Asthma
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
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
0.700 1.000 1 2019 2019
dbSNP: rs3828805
rs3828805
0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv
Malignant neoplasm of lateral floor of mouth
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
0.700 1.000 1 2016 2016
dbSNP: rs3828805
rs3828805
0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv
CUI: C0153382
Disease: Malignant neoplasm of oropharynx
Malignant neoplasm of oropharynx
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 other specified parts of mouth
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 other sites within the lip and oral cavity
0.700 1.000 1 2016 2016
dbSNP: rs3828805
rs3828805
0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv
CUI: C0031347
Disease: Pharyngeal Neoplasms
Pharyngeal Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs3828805
rs3828805
0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.700 1.000 1 2016 2016
dbSNP: rs3828805
rs3828805
0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv
CUI: C2349952
Disease: Oropharyngeal Carcinoma
Oropharyngeal Carcinoma
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 posterior wall of oropharynx
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 wall of oropharynx
0.700 1.000 1 2016 2016