Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs1495743 8 18415790 intergenic variant G/A;C snv 6
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv 3
rs1203936 20 22611792 upstream gene variant G/C;T snv 2
rs13391552
ALMS1
2 73591809 intron variant G/A;C snv 2
rs1349497
RAPGEF4-AS1
2 172727935 intron variant G/A;C snv 2
rs2403254
HPS5
11 18303599 intron variant C/G;T snv 2
rs2411884
KCNQ1
11 2714304 intron variant C/A;G snv 2
rs2518049
AKR1C3
10 5095844 intron variant A/G;T snv 2
rs4329
ACE
17 63486097 intron variant A/C;G snv 2
rs4581570 13 27936575 intergenic variant T/A;C snv 2