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: rs2073498
rs2073498
0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
Neoplasms 0.010 1.000 1 2006 2006
dbSNP: rs1208415127
rs1208415127
0.827 0.160 3 50331654 missense variant G/A snv 4.0E-06
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2073498
rs2073498
0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1208415127
rs1208415127
0.827 0.160 3 50331654 missense variant G/A snv 4.0E-06
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2073498
rs2073498
0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2006 2014
dbSNP: rs1989839
rs1989839
0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1208415127
rs1208415127
0.827 0.160 3 50331654 missense variant G/A snv 4.0E-06
CUI: C4048328
Disease: cervical cancer
cervical cancer
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2005 2005
dbSNP: rs1989839
rs1989839
0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma
Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs2236947
rs2236947
0.882 0.040 3 50334001 intron variant C/A snv 0.39
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma
Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs200913791
rs200913791
0.925 0.160 3 50342473 missense variant A/G snv 2.0E-04 3.5E-05
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs200913791
rs200913791
0.925 0.160 3 50342473 missense variant A/G snv 2.0E-04 3.5E-05
CUI: C3809543
Disease: CILIARY DYSKINESIA, PRIMARY, 22
CILIARY DYSKINESIA, PRIMARY, 22
0.800 1.000 4 2013 2018
dbSNP: rs397515460
rs397515460
1.000 3 50342047 stop gained G/A snv 8.0E-06 7.0E-06
CUI: C3809543
Disease: CILIARY DYSKINESIA, PRIMARY, 22
CILIARY DYSKINESIA, PRIMARY, 22
0.700 0
dbSNP: rs753061612
rs753061612
1.000 3 50341685 missense variant T/C snv 1.2E-05
CUI: C3809543
Disease: CILIARY DYSKINESIA, PRIMARY, 22
CILIARY DYSKINESIA, PRIMARY, 22
0.700 0
dbSNP: rs1297857806
rs1297857806
3 50342917 splice donor variant C/T snv 4.0E-06
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.700 1.000 2 2013 2013
dbSNP: rs200913791
rs200913791
0.925 0.160 3 50342473 missense variant A/G snv 2.0E-04 3.5E-05
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2073498
rs2073498
0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis
Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1389001294
rs1389001294
1.000 0.040 3 50331640 missense variant C/T snv 1.4E-05
CUI: C0206624
Disease: Hepatoblastoma
Hepatoblastoma
Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs1208415127
rs1208415127
0.827 0.160 3 50331654 missense variant G/A snv 4.0E-06
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2073498
rs2073498
0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs2073498
rs2073498
0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs2073498
rs2073498
0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2006 2014
dbSNP: rs1208415127
rs1208415127
0.827 0.160 3 50331654 missense variant G/A snv 4.0E-06
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1989839
rs1989839
0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1184094026
rs1184094026
0.925 0.080 3 50331675 missense variant T/G snv 8.0E-06 1.4E-05
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1208415127
rs1208415127
0.827 0.160 3 50331654 missense variant G/A snv 4.0E-06
Malignant neoplasm of urinary bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2010 2010