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: rs8045064
rs8045064
1.000 0.080 16 24664268 intron variant T/C snv 3.5E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.800 1.000 1 2014 2014
dbSNP: rs34172651
rs34172651
16 24755520 intron variant T/C snv 0.35
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 3 2018 2019
dbSNP: rs2188717
rs2188717
16 24718909 intron variant T/A;C snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2019 2019
dbSNP: rs7188873
rs7188873
16 24715743 intron variant A/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 2 2018 2019
dbSNP: rs112927956
rs112927956
16 24712680 intron variant C/T snv 2.8E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2019 2019
dbSNP: rs11639856
rs11639856
1.000 0.040 16 24777324 missense variant T/A snv 0.17 0.19
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2016 2016
dbSNP: rs11639856
rs11639856
1.000 0.040 16 24777324 missense variant T/A snv 0.17 0.19
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs12596320
rs12596320
1.000 0.040 16 24806184 intron variant C/T snv 7.6E-02 4.2E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs12599552
rs12599552
1.000 0.040 16 24794853 intron variant T/A snv 6.3E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs12708665
rs12708665
16 24716906 intron variant A/G snv 0.74
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs13336754
rs13336754
1.000 0.040 16 24790658 missense variant C/A;G;T snv 4.0E-06; 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs1465423
rs1465423
1.000 0.040 16 24761359 intron variant G/C snv 0.18
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs17177078
rs17177078
1.000 0.040 16 24799360 intron variant C/T snv 4.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs200528
rs200528
1.000 0.040 16 24747810 intron variant A/G snv 0.82
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.700 1.000 1 2019 2019
dbSNP: rs200528
rs200528
1.000 0.040 16 24747810 intron variant A/G snv 0.82
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2019 2019
dbSNP: rs200541
rs200541
16 24721820 intron variant A/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2017 2017
dbSNP: rs2059134
rs2059134
1.000 0.040 16 24805171 non coding transcript exon variant A/G snv 0.25 0.27
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs2112783
rs2112783
1.000 0.040 16 24801191 intron variant G/A snv 0.13
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs2112784
rs2112784
1.000 0.040 16 24770629 intron variant G/A snv 2.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs2287786
rs2287786
1.000 0.040 16 24806487 intron variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs28512462
rs28512462
16 24700485 intron variant C/A;G snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs3803716
rs3803716
1.000 0.040 16 24791004 missense variant C/T snv 0.17 0.18
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs6497755
rs6497755
1.000 0.040 16 24775874 intron variant C/A snv 0.60
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs7186893
rs7186893
16 24795099 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs7186893
rs7186893
16 24795099 intron variant G/A;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019