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: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.900 0.902 122 1997 2018
dbSNP: rs1899951
rs1899951
0.851 0.160 3 12353341 intron variant C/T snv 0.26
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.800 1.000 2 2012 2018
dbSNP: rs72551363
rs72551363
0.882 0.080 3 12417048 missense variant T/A snv
Familial Partial Lipodystrophy, Type 3
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.800 1.000 2 2002 2002
dbSNP: rs72551364
rs72551364
0.851 0.160 3 12433900 missense variant C/T snv
Familial Partial Lipodystrophy, Type 3
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.800 1.000 2 2002 2002
dbSNP: rs121909244
rs121909244
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06
Familial Partial Lipodystrophy, Type 3
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.700 1.000 4 2000 2014
dbSNP: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 3 2012 2018
dbSNP: rs1699337
rs1699337
3 12408594 intron variant G/A;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2015 2018
dbSNP: rs2960422
rs2960422
1.000 0.080 3 12293492 intron variant G/A snv 0.59
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 2 2016 2019
dbSNP: rs10510418
rs10510418
1.000 0.040 3 12347064 intron variant A/C snv 0.25
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10510419
rs10510419
3 12385437 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs10865710
rs10865710
0.763 0.360 3 12311699 intron variant C/G snv 0.25
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11128597
rs11128597
1.000 0.040 3 12303137 intron variant A/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11128598
rs11128598
1.000 0.040 3 12311827 intron variant T/C snv 0.25
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11709077
rs11709077
0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs11709077
rs11709077
0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2015 2015
dbSNP: rs11709077
rs11709077
0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11710969
rs11710969
1.000 0.040 3 12302092 intron variant G/A snv 0.28
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11712037
rs11712037
3 12303231 intron variant C/G snv 9.2E-02
body fat percentage (physical finding)
0.700 1.000 1 2019 2019
dbSNP: rs11715073
rs11715073
0.925 0.120 3 12311472 intron variant C/G snv 0.25
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs117350179
rs117350179
3 12332833 intron variant C/G snv 2.9E-02
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs12485478
rs12485478
1.000 0.040 3 12309724 intron variant A/G snv 3.8E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12490265
rs12490265
1.000 0.040 3 12343043 intron variant G/A snv 0.25
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12493718
rs12493718
1.000 0.040 3 12322138 intron variant G/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12495364
rs12495364
1.000 0.040 3 12320430 intron variant T/C snv 0.27
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12629751
rs12629751
3 12357908 intron variant C/T snv 7.6E-02
CUI: C0202194
Disease: Potassium measurement
Potassium measurement
0.700 1.000 1 2018 2018