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: rs3828805
rs3828805 		0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv
CUI: C0496758
Disease: Malignant neoplasm of lateral floor of mouth
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
CUI: C0153369
Disease: Malignant neoplasm of anterior portion of floor of mouth
Malignant neoplasm of anterior portion 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
CUI: C0031347
Disease: Pharyngeal Neoplasms
Pharyngeal Neoplasms 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic 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
CUI: C0153382
Disease: Malignant neoplasm of oropharynx
Malignant neoplasm of oropharynx 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic 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
CUI: C0153389
Disease: malignant neoplasm of lateral wall of oropharynx
malignant neoplasm of lateral wall of oropharynx 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic 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
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm 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
CUI: C0153407
Disease: Malignant neoplasm of other sites within the lip and oral cavity
Malignant neoplasm of other sites within the lip and oral cavity 		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
CUI: C2349952
Disease: Oropharyngeal Carcinoma
Oropharyngeal Carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic 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
CUI: C0153380
Disease: Malignant neoplasm of other specified parts of mouth
Malignant neoplasm of other specified parts 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
CUI: C0153390
Disease: Malignant neoplasm of posterior wall of oropharynx
Malignant neoplasm of posterior wall of oropharynx 		Neoplasms; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic 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
CUI: C3165521
Disease: Primary malignant neoplasm of lateral wall of oropharynx
Primary malignant neoplasm of lateral wall of oropharynx 		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: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
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 		Digestive System Diseases 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: C0241910
Disease: Autoimmune Chronic Hepatitis
Autoimmune Chronic Hepatitis 		Digestive System Diseases; Immune System Diseases 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: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs3891175
rs3891175 		0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20
CUI: C1332355
Disease: Autoimmune Hepatitis with Centrilobular Necrosis
Autoimmune Hepatitis with Centrilobular Necrosis 		0.700 1.000 1 2018 2018
dbSNP: rs41563814
rs41563814 		1.000 0.040 6 32664881 missense variant A/T snv 3.2E-05
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2016 2016
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: rs4713572
rs4713572 		6 32659175 upstream gene variant T/A;C snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4988888
rs4988888 		1.000 0.040 6 32667420 intron variant T/C snv 0.20
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		Hemic and Lymphatic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs77296290
rs77296290 		1.000 0.040 6 32667519 intron variant C/T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs9273401
rs9273401 		1.000 0.080 6 32659352 upstream gene variant A/G snv 0.10
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs9273404
rs9273404 		1.000 0.040 6 32659383 upstream gene variant A/G snv 0.56
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9273410
rs9273410 		1.000 0.080 6 32659473 3 prime UTR variant C/A snv 0.51
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9273542
rs9273542 		6 32661035 intron variant C/A;T snv
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2019 2019