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: 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: 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: 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: 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: rs9273552
rs9273552
6 32661139 intron variant G/A snv 1.8E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
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: 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: rs9274600
rs9274600
6 32667815 intron variant A/G snv 0.43
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2015 2015
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: 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