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: 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: 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: 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
dbSNP: rs3828805
rs3828805
0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv
Primary malignant neoplasm of lateral 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 floor of mouth
0.700 1.000 1 2016 2016
dbSNP: rs3891175
rs3891175
0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
Autoimmune Chronic Hepatitis
0.700 1.000 1 2018 2018
dbSNP: rs3891175
rs3891175
0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2018 2018
dbSNP: rs3891175
rs3891175
0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20
Autoimmune Hepatitis with Centrilobular Necrosis
0.700 1.000 1 2018 2018
dbSNP: rs4642515
rs4642515
6 32664039 non coding transcript exon variant T/A;G snv
CUI: C1277709
Disease: Transferrin saturation measurement
Transferrin saturation measurement
0.700 1.000 1 2017 2017
dbSNP: rs77296290
rs77296290
1.000 0.040 6 32667519 intron variant C/T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2019 2019
dbSNP: rs9274247
rs9274247
6 32663518 non coding transcript exon variant G/A;T snv 0.35
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs9274247
rs9274247
6 32663518 non coding transcript exon variant G/A;T snv 0.35
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2019 2019
dbSNP: rs9274299
rs9274299
1.000 0.040 6 32664181 non coding transcript exon variant C/A;G;T snv 1.7E-03
Child Development Disorders, Pervasive
0.700 1.000 1 2017 2017
dbSNP: rs9274299
rs9274299
1.000 0.040 6 32664181 non coding transcript exon variant C/A;G;T snv 1.7E-03
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2017 2017