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: rs12429545
rs12429545
13 53528071 intron variant G/A;T snv 0.12
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 10 2015 2019
dbSNP: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snv 0.50
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 10 2010 2019
dbSNP: rs13021737
rs13021737
2 632348 intergenic variant A/G snv 0.85
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 8 2015 2019
dbSNP: rs1354034
rs1354034
3 56815721 intron variant T/C snv 0.49
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 8 2011 2019
dbSNP: rs10132280
rs10132280
14 25458973 intergenic variant C/A snv 0.37
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs1327235
rs1327235
20 10988382 intron variant A/G snv 0.46
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 7 2011 2018
dbSNP: rs17024393
rs17024393
1 109612066 intron variant T/C snv 4.6E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs17405819
rs17405819
8 75894349 intergenic variant T/C snv 0.24
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs1928295
rs1928295
9 117616205 intergenic variant T/C snv 0.45
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs2365389
rs2365389
3 61250788 intron variant C/T snv 0.56
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2018
dbSNP: rs445
rs445
7 92779056 intron variant C/T snv 0.14
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.800 1.000 7 2010 2019
dbSNP: rs6864049
rs6864049
5 124994829 intron variant A/C;G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 7 2015 2019
dbSNP: rs11165643
rs11165643
1 96458541 intergenic variant C/T snv 0.48
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 6 2015 2019
dbSNP: rs1167827
rs1167827
7 75533848 3 prime UTR variant G/A snv 0.37
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 6 2015 2018
dbSNP: rs11953630
rs11953630
5 158418394 intergenic variant C/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 6 2011 2018
dbSNP: rs12885454
rs12885454
14 29267632 non coding transcript exon variant C/A snv 0.27
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 6 2015 2019
dbSNP: rs13191362
rs13191362
6 162612318 intron variant A/G snv 8.7E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 6 2015 2019
dbSNP: rs13209747
rs13209747
6 126794309 intron variant C/G;T snv 0.36
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 6 2013 2018
dbSNP: rs16907751
rs16907751
8 80463222 intron variant C/T snv 0.10
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 6 2015 2019
dbSNP: rs17080102
rs17080102
6 150683634 5 prime UTR variant G/C snv 8.6E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 6 2013 2019
dbSNP: rs2033529
rs2033529
6 40380914 intron variant A/C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 6 2015 2019
dbSNP: rs2068888
rs2068888
10 93079885 downstream gene variant G/A snv 0.42
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 6 2010 2019
dbSNP: rs2228213
rs2228213
6 12124622 missense variant G/A snv 0.30 0.26
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 6 2015 2019
dbSNP: rs2284746
rs2284746
1 16980180 intron variant C/A;G snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 6 2010 2019
dbSNP: rs35444
rs35444
12 115114632 intergenic variant A/G snv 0.38
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 6 2011 2019