Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs1126930
PRKAG1 ; DDN-AS1
12 49005349 missense variant G/C snv 2.1E-02 2.1E-02 5
rs113191842
FTO
16 53783406 intron variant G/A snv 9.4E-02 5
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 5
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 5
rs12140153
PATJ
1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02 5
rs12902602
LOC112268142 ; CHRNB4
15 78675059 intron variant A/G snv 0.28 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5