Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 9
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 9
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs3741378
SIPA1
0.851 0.080 11 65641466 missense variant C/G;T snv 0.15 8
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 7
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 6
rs757110
ABCC8
0.851 0.080 11 17396930 missense variant C/A;T snv 0.64; 8.0E-06 6
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs12140153
PATJ
1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02 5
rs634869 6 139510620 intron variant T/A;C snv 5
rs10842707 12 26318431 intron variant C/G;T snv 4
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs17819328 3 12447843 intergenic variant T/A;G snv 4
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82 4
rs2033529
TDRG1
6 40380914 intron variant A/C;G snv 4
rs6545714 2 59080590 intron variant G/A;C snv 4
rs757608 17 61419916 regulatory region variant A/G;T snv 4