Source: GWASCAT

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: rs11709077
rs11709077
0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2012 2012
dbSNP: rs17036170
rs17036170
1.000 0.080 3 12288912 5 prime UTR variant G/A snv 1.1E-02
Chemical and Drug Induced Liver Injury
0.700 1.000 1 2012 2012
dbSNP: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 1 2012 2012
dbSNP: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
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: rs17036328
rs17036328
1.000 0.040 3 12348985 intron variant T/C snv 0.14
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2016 2016
dbSNP: rs17036328
rs17036328
1.000 0.040 3 12348985 intron variant T/C snv 0.14
CUI: C4049919
Disease: Insulin Sensitivity Measurement
Insulin Sensitivity Measurement
0.700 1.000 1 2016 2016
dbSNP: rs4073770
rs4073770
3 12326734 intron variant A/T snv 0.25
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs6442310
rs6442310
3 12316731 intron variant T/A snv 0.66
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
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
0.700 1.000 1 2017 2017
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
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
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
0.700 1.000 1 2017 2017
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
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
0.700 1.000 1 2017 2017
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
0.700 1.000 1 2017 2017
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
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
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
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
0.700 1.000 1 2017 2017
dbSNP: rs12633551
rs12633551
3 12318995 intron variant C/T snv 2.8E-02
High density lipoprotein measurement
0.700 1.000 1 2017 2017
dbSNP: rs13061415
rs13061415
1.000 0.040 3 12308425 intron variant T/C snv 0.28
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17036188
rs17036188
0.882 0.120 3 12299426 intron variant T/C snv 4.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17036326
rs17036326
1.000 0.040 3 12347814 intron variant A/G snv 0.14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17036328
rs17036328
1.000 0.040 3 12348985 intron variant T/C snv 0.14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017