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: rs1130399
rs1130399
1.000 0.040 6 32661978 missense variant G/A;T snv 0.20
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.010 1.000 1 2017 2017
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: 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: 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: 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: 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
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
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
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
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
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
Primary malignant neoplasm of lateral wall of oropharynx
0.700 1.000 1 2016 2016
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: 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: 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
dbSNP: rs9273643
rs9273643
0.925 0.120 6 32661407 missense variant A/G snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2000 2000