Source: CURATED

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: rs3887275
rs3887275
1.000 0.080 22 29904123 intron variant C/G snv 0.22
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.700 1.000 1 2011 2011
dbSNP: rs39713
rs39713
1.000 0.040 22 29947197 intron variant C/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs41158
rs41158
1.000 0.040 22 30009994 non coding transcript exon variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs41159
rs41159
1.000 0.040 22 30011375 non coding transcript exon variant G/A snv 0.65
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs41164
rs41164
1.000 0.040 22 30016476 non coding transcript exon variant T/C snv 0.28
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs41170
rs41170
1.000 0.040 22 30025077 non coding transcript exon variant A/G snv 0.72
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs41172
rs41172
1.000 0.080 22 30026876 3 prime UTR variant T/C snv 0.28
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.700 1.000 1 2011 2011
dbSNP: rs41278853
rs41278853
1.000 0.080 22 30020538 missense variant A/G;T snv 5.8E-02; 4.0E-06
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2018 2018
dbSNP: rs4239932
rs4239932
1.000 0.080 22 29972395 intron variant T/G snv 0.78
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.700 1.000 1 2011 2011
dbSNP: rs4823063
rs4823063
1.000 0.080 22 29912791 intron variant G/C snv 0.21
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.700 1.000 1 2011 2011
dbSNP: rs5752989
rs5752989
22 29969791 intron variant G/A;T snv
CUI: C0424678
Disease: Lean body mass
Lean body mass
0.700 1.000 1 2019 2019
dbSNP: rs5763609
rs5763609
1.000 0.040 22 29927101 intron variant G/A snv 5.7E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs5763646
rs5763646
22 29963421 intron variant T/C snv 0.38
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs5763662
rs5763662
22 29982714 non coding transcript exon variant C/T snv 3.7E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2013 2013
dbSNP: rs5763674
rs5763674
0.925 0.120 22 29990369 non coding transcript exon variant C/T snv 0.78
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.700 1.000 1 2017 2017
dbSNP: rs5763674
rs5763674
0.925 0.120 22 29990369 non coding transcript exon variant C/T snv 0.78
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
0.700 1.000 1 2017 2017
dbSNP: rs5763681
rs5763681
1.000 0.040 22 29993857 non coding transcript exon variant C/T snv 5.7E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs5763688
rs5763688
1.000 0.040 22 29997514 non coding transcript exon variant C/A;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs6006310
rs6006310
22 29952410 intron variant G/T snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2016 2016
dbSNP: rs713718
rs713718
1.000 0.040 22 29918103 intron variant T/G snv 0.37
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs7284538
rs7284538
1.000 0.040 22 29979545 non coding transcript exon variant A/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs7285751
rs7285751
1.000 0.040 22 29997555 non coding transcript exon variant C/G snv 0.15
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs737903
rs737903
1.000 0.040 22 29947857 intron variant T/A snv 5.4E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs737904
rs737904
1.000 0.040 22 29952663 intron variant A/T snv 0.79
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs737909
rs737909
0.925 0.080 22 29992769 non coding transcript exon variant T/G snv 0.73
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017