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: rs12507026
rs12507026
4 45179317 intergenic variant A/C;T snv 0.37
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs12681792
rs12681792
8 61141904 intron variant C/A snv 0.23
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs1285245
rs1285245
17 79823090 non coding transcript exon variant G/C snv 0.45
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs1285997
rs1285997
14 91046685 intron variant C/A;G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs13033310
rs13033310
2 132766032 intron variant G/A snv 0.27
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs1320251
rs1320251
17 21361084 regulatory region variant C/T snv 0.49
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs1320903
rs1320903
3 132039233 intron variant G/A snv 0.31
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs13264909
rs13264909
8 63789828 intron variant A/T snv 0.49
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs1363695
rs1363695
5 131042334 intergenic variant C/T snv 0.20
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs140733155
rs140733155
21 46628861 intergenic variant A/G snv 9.3E-03
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs1477890
rs1477890
4 18510115 intron variant A/G snv 0.45
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs148108087
rs148108087
19 51278201 intron variant G/A snv 3.4E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs148636479
rs148636479
4 163438526 intergenic variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs1658820
rs1658820
8 4431055 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs16906845
rs16906845
8 137202985 intergenic variant G/A snv 0.10
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs16989232
rs16989232
20 40663144 intergenic variant G/A snv 0.45
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs17193211
rs17193211
21 37513203 3 prime UTR variant C/T snv 5.5E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs1787267
rs1787267
18 78982544 intron variant G/C snv 9.2E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs1852006
rs1852006
7 78200451 intron variant G/A snv 0.37
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs1884389
rs1884389
20 1429938 regulatory region variant C/T snv 0.41
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs192829047
rs192829047
5 173850244 regulatory region variant T/C snv 9.0E-03
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs194809
rs194809
16 23793635 intergenic variant G/A snv 0.16
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs1982441
rs1982441
8 28164252 intron variant G/T snv 9.7E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs2051559
rs2051559
4 3297073 intron variant T/C snv 0.12
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs2072597
rs2072597
19 12885926 missense variant A/G snv 0.37 0.36
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019